The following data is part of a premarket notification filed by Cardiovascular Imaging Systems, Inc. with the FDA for Cvis Insight Imaging Guide Catheter.
| Device ID | K930232 |
| 510k Number | K930232 |
| Device Name: | CVIS INSIGHT IMAGING GUIDE CATHETER |
| Classification | Catheter, Intravascular, Diagnostic |
| Applicant | CARDIOVASCULAR IMAGING SYSTEMS, INC. 595 NORTH PASTORIA AVE. Sunnyvale, CA 94085 |
| Contact | Stan E Tillman |
| Correspondent | Stan E Tillman 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 | 1993-01-19 |
| Decision Date | 1993-07-21 |