The following data is part of a premarket notification filed by Pie Medical Imaging B.v. with the FDA for Caas A-valve.
Device ID | K113076 |
510k Number | K113076 |
Device Name: | CAAS A-VALVE |
Classification | System, Image Processing, Radiological |
Applicant | PIE MEDICAL IMAGING B.V. BECANUSSTRAAT 13 D Maastricht, NL 6216 Bx |
Contact | Florie Daniels |
Correspondent | Florie Daniels PIE MEDICAL IMAGING B.V. BECANUSSTRAAT 13 D Maastricht, NL 6216 Bx |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-10-17 |
Decision Date | 2012-01-30 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
08056304451149 | K113076 | 000 |