The following data is part of a premarket notification filed by Target Therapeutics with the FDA for Diagnostic Intravascular Catheter.
| Device ID | K925813 |
| 510k Number | K925813 |
| Device Name: | DIAGNOSTIC INTRAVASCULAR CATHETER |
| Classification | Catheter, Intravascular, Diagnostic |
| Applicant | TARGET THERAPEUTICS 47201 LAKEVIEW BLVD. P.O. BOX 5120 Freemont, CA 94538 |
| Contact | Laraine Pangelina |
| Correspondent | Laraine Pangelina TARGET THERAPEUTICS 47201 LAKEVIEW BLVD. P.O. BOX 5120 Freemont, CA 94538 |
| Product Code | DQO |
| CFR Regulation Number | 870.1200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-11-17 |
| Decision Date | 1994-03-23 |