Apparatus, Suction, Ward Use, Portable, Ac-powered

Device Code: 5689

Product Code(s): JCX

Device Classification Information

Device Type ID5689
Device NameApparatus, Suction, Ward Use, Portable, Ac-powered
Regulation DescriptionPowered Suction Pump.
Regulation Medical SpecialtyGeneral & Plastic Surgery
Review PanelGeneral & Plastic Surgery
Premarket Review Office Of Device Evaluation (ODE)
Division Of Surgical Devices (DSD)
General Surgery Devices Branch Two - Surgical (GSDB2)
Submission Type510(k)
CFR Regulation Number878.4780 [🔎]
FDA Device ClassificationClass 2 Medical Device
Product CodeJCX
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 ID5689
DeviceApparatus, Suction, Ward Use, Portable, Ac-powered
Product CodeJCX
FDA Device ClassificationClass 2 Medical Device
Regulation DescriptionPowered Suction Pump.
CFR Regulation Number878.4780 [🔎]
Premarket Reviews
ManufacturerDecision
DING HWA CO., LTD
 
SUBSTANTIALLY EQUIVALENT
1
DING HWA CO., LTD.
 
SUBSTANTIALLY EQUIVALENT
2
IMPACT INSTRUMENTATION, INC.
 
SUBSTANTIALLY EQUIVALENT
1
STRYKER CORP.
 
SUBSTANTIALLY EQUIVALENT
1
STRYKER CORPORATION
 
SUBSTANTIALLY EQUIVALENT
1
ZIMMER, INC.
 
SUBSTANTIALLY EQUIVALENT
1
Device Problems
Device Emits Odor
58
No Pressure
47
Smoking
43
Fluid Leak
36
Device Operates Differently Than Expected
31
Suction Problem
30
Device Operational Issue
29
Aspiration Issue
29
Filtration Problem
23
Sparking
22
Device Handling Problem
19
Failure To Pump
18
Complete Blockage
17
Pressure Problem
16
Leak / Splash
16
Electrical /Electronic Property Problem
15
Failure To Power Up
14
Pumping Problem
11
Noise, Audible
10
Incorrect, Inadequate Or Imprecise Result Or Readings
10
Misconnection
10
Device Contamination With Body Fluid
10
Overheating Of Device
9
Device Damaged Prior To Use
8
Incorrect Measurement
8
Pumping Stopped
6
Mechanical Problem
6
Output Problem
5
Unable To Obtain Readings
5
Appropriate Term/Code Not Available
5
Connection Problem
4
Inappropriate Shock
4
Improper Device Output
4
Cut In Material
4
Decrease In Suction
3
Inaccurate Information
3
Device Stops Intermittently
3
Contamination During Use
3
Improper Or Incorrect Procedure Or Method
3
Material Frayed
3
Use Of Device Problem
3
Melted
2
Occlusion Within Device
2
Device Displays Incorrect Message
2
Power Problem
2
Fire
2
Decrease In Pressure
2
Electrical Shorting
2
Device Alarm System
2
Thermal Decomposition Of Device
2
Break
2
Improper Flow Or Infusion
2
Temperature Problem
1
Failure To Run On AC/DC
1
Charred
1
Defective Device
1
Detachment Of Device Or Device Component
1
Failure To Shut Off
1
No Audible Prompt / Feedback
1
Failure To Zero
1
Failure To Obtain Sample
1
Detachment Of Device Component
1
Air Leak
1
Off-Label Use
1
Excess Flow Or Over-Infusion
1
Pre Or Post-Pumping Problem
1
Failure To Sense
1
Infusion Or Flow Problem
1
Device Fell
1
Suction Failure
1
Material Integrity Problem
1
Low Readings
1
Battery Problem
1
Device Inoperable
1
Power Conditioning Problem
1
Adverse Event Without Identified Device Or Use Problem
1
Backflow
1
Bacterial Filter
1
Difficult To Open Or Close
1
Device Dislodged Or Dislocated
1
Increase In Suction
1
Total Device Problems 654
Recalls
Manufacturer Recall Class Date Posted
1
DeVilbiss Healthcare LLC
II Jul-20-2016
2
EMG Technology Co., Ltd.
II Sep-13-2014
3
Gardner Denver Thomas Inc
II Jul-20-2015
4
Laerdal Medical Corporation
II Mar-12-2018
5
Laerdal Medical Corporation
II Apr-20-2017
6
Stryker Instruments Div. Of Stryker Corporation
II Aug-23-2016
7
Stryker Instruments Div. Of Stryker Corporation
II Jul-17-2015
8
Stryker Instruments Div. Of Stryker Corporation
II Jan-31-2014
TPLC Last Update: 2019-04-02 21:10:52

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