The following data is part of a premarket notification filed by Pie Medical Imaging Bv with the FDA for Caas Mrv.
Device ID | K162112 |
510k Number | K162112 |
Device Name: | CAAS MRV |
Classification | System, Image Processing, Radiological |
Applicant | Pie Medical Imaging BV Philipsweg 1 Maastricht, NL 6227 Aj |
Contact | Annemiek Bouts |
Correspondent | Annemiek Bouts Pie Medical Imaging BV Philipsweg 1 Maastricht, NL 6227 Aj |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-07-29 |
Decision Date | 2016-09-21 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
08056304453426 | K162112 | 000 |
08056304453044 | K162112 | 000 |