System, X-ray, Angiographic

Device Code: 5342

Product Code(s): IZI

Device Classification Information

Device Type ID5342
Device NameSystem, X-ray, Angiographic
Regulation DescriptionAngiographic X-ray System.
Regulation Medical SpecialtyRadiology
Review PanelRadiology
Premarket Review Office Of In Vitro Diagnostics And Radiological Health (OIR)
Submission Type510(k)
CFR Regulation Number892.1600 [🔎]
FDA Device ClassificationClass 2 Medical Device
Product CodeIZI
GMP ExemptNo
Summary MREligible
Implanted DeviceNo
Life Support DeviceNo
Third Party Review Eligible For Accredited Persons Program

Recognized Standards

Total Product Life Cycle

Device Type ID5342
DeviceSystem, X-ray, Angiographic
Product CodeIZI
FDA Device ClassificationClass 2 Medical Device
Regulation DescriptionAngiographic X-ray System.
CFR Regulation Number892.1600 [🔎]
Premarket Reviews
ManufacturerDecision
CARL ZEISS MEDITEC INC
 
SUBSTANTIALLY EQUIVALENT - WITH DRUG
1
CARL ZEISS MEDITEC, INC.
 
SUBSTANTIALLY EQUIVALENT - WITH DRUG
1
HAMAMATSU PHOTONICS, K.K.
 
SUBSTANTIALLY EQUIVALENT
1
LEICA MICROSYSTEMS CMS GMBH
 
SUBSTANTIALLY EQUIVALENT
1
 
SUBSTANTIALLY EQUIVALENT - KIT WITH DRUGS
1
LEICA MICROSYSTEMS, INC.
 
SUBSTANTIALLY EQUIVALENT - KIT WITH DRUGS
1
 
SUBSTANTIALLY EQUIVALENT
2
MIVENION GMBH
 
SUBSTANTIALLY EQUIVALENT
1
PIE MEDICAL IMAGING
 
SUBSTANTIALLY EQUIVALENT
1
PIE MEDICAL IMAGING B.V.
 
SUBSTANTIALLY EQUIVALENT
1
Device Problems
Insufficient Information
45
No Apparent Adverse Event
11
Missing Value Reason
4
Component Falling
3
Detachment Of Device Component
3
Loss Of Power
3
Device Displays Incorrect Message
3
Device Operates Differently Than Expected
3
Device Operational Issue
2
Bent
2
Device Stops Intermittently
2
Device Inoperable
2
Improper Or Incorrect Procedure Or Method
2
Power Problem
2
Adverse Event Without Identified Device Or Use Problem
2
Computer Operating System Problem
2
System
2
Repair
1
Use Of Incorrect Control Settings
1
Device Contamination With Chemical Or Other Material
1
Unintended Movement
1
Loose Or Intermittent Connection
1
Other (for Use When An Appropriate Device Code Cannot Be Identified)
1
Temperature Problem
1
Computer Hardware
1
Foot Pedal
1
Electrical /Electronic Property Problem
1
Self-Activation Or Keying
1
Appropriate Term/Code Not Available
1
Use Of Device Problem
1
Radiation Overexposure
1
Data Problem
1
CRT (Cathode Ray Tube)
1
Failure To Fire
1
Foot Switch
1
Human-Device Interface Problem
1
Total Device Problems 112
Recalls
Manufacturer Recall Class Date Posted
1
GE Healthcare
II Jul-03-2015
2
GE Healthcare, LLC
II Dec-23-2016
3
GE Healthcare, LLC
II Dec-16-2014
4
GE Healthcare, LLC
II Jan-28-2014
5
GE Medical Systems, LLC
II Dec-12-2015
6
NOVADAQ TECHNOLOGIES INC.
II Sep-08-2016
7
NeuroLogica Corporation
II Nov-10-2015
8
Novadaq Technologies, Inc.
III Dec-01-2014
9
Philips Electronics North America Corporation
II Sep-21-2018
10
Philips Electronics North America Corporation
II Jan-20-2017
11
Philips Electronics North America Corporation
II Jan-20-2017
12
Philips Electronics North America Corporation
II Aug-01-2016
13
Philips Electronics North America Corporation
II Feb-16-2016
14
Philips Electronics North America Corporation
II Jan-30-2016
15
Philips Medical Systems Nederlands
II May-03-2018
16
Philips Medical Systems, Inc.
II Mar-31-2016
17
Philips Medical Systems, Inc.
II Mar-02-2015
18
Philips Medical Systems, Inc.
II Feb-26-2015
19
Philips North America, LLC
II Mar-23-2019
20
Shimadzu Medical Systems
II Jun-14-2018
21
Shimadzu Medical Systems
II May-08-2014
22
Shimadzu Medical Systems Usa Com
II Feb-27-2019
23
Siemens Medical Solutions USA, Inc
II Dec-05-2018
24
Siemens Medical Solutions USA, Inc
II Nov-14-2018
25
Siemens Medical Solutions USA, Inc
II Feb-23-2018
26
Siemens Medical Solutions USA, Inc
II Aug-29-2017
27
Siemens Medical Solutions USA, Inc
II Jul-14-2017
28
Siemens Medical Solutions USA, Inc
II Mar-30-2017
29
Siemens Medical Solutions USA, Inc
II Mar-14-2017
30
Siemens Medical Solutions USA, Inc
II Aug-11-2016
31
Siemens Medical Solutions USA, Inc
II Aug-05-2016
32
Siemens Medical Solutions USA, Inc
II Mar-31-2016
33
Siemens Medical Solutions USA, Inc
II Mar-31-2016
34
Siemens Medical Solutions USA, Inc
II Mar-31-2016
35
Siemens Medical Solutions USA, Inc
II Aug-05-2015
36
Siemens Medical Solutions USA, Inc
II Jan-14-2015
37
Siemens Medical Solutions USA, Inc
II Dec-01-2014
38
Siemens Medical Solutions USA, Inc
II Nov-07-2014
39
Siemens Medical Solutions USA, Inc
II Sep-24-2014
40
Siemens Medical Solutions USA, Inc
II Sep-22-2014
41
Siemens Medical Solutions USA, Inc
II Mar-31-2014
42
Siemens Medical Solutions USA, Inc
II Mar-22-2014
43
Siemens Medical Solutions USA, Inc
II Feb-24-2014
TPLC Last Update: 2019-04-02 21:04:39

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.