The following data is part of a premarket notification filed by Cardiovascular Imaging Systems, Inc. with the FDA for Cvis Insight Imaging Catheter.
Device ID | K904618 |
510k Number | K904618 |
Device Name: | CVIS INSIGHT IMAGING CATHETER |
Classification | Catheter, Intravascular, Diagnostic |
Applicant | CARDIOVASCULAR IMAGING SYSTEMS, INC. 595 NORTH PASTORIA AVE. Sunnyvale, CA 94085 |
Contact | Russell W Felkey |
Correspondent | Russell W Felkey CARDIOVASCULAR IMAGING SYSTEMS, INC. 595 NORTH PASTORIA AVE. Sunnyvale, CA 94085 |
Product Code | DQO |
CFR Regulation Number | 870.1200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-10-11 |
Decision Date | 1991-04-12 |