CAAS WORKSTATION

System, X-ray, Angiographic

PIE MEDICAL IMAGING

The following data is part of a premarket notification filed by Pie Medical Imaging with the FDA for Caas Workstation.

Pre-market Notification Details

Device IDK133993
510k NumberK133993
Device Name:CAAS WORKSTATION
ClassificationSystem, X-ray, Angiographic
Applicant PIE MEDICAL IMAGING PHILIPSWEG 1 Maastricht, Limburg,  NL 6227 Aj
ContactFlorie Daniels
CorrespondentFlorie Daniels
PIE MEDICAL IMAGING PHILIPSWEG 1 Maastricht, Limburg,  NL 6227 Aj
Product CodeIZI  
CFR Regulation Number892.1600 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2013-12-26
Decision Date2014-03-25
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
08056304451194 K133993 000

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