The following data is part of a premarket notification filed by Primrose Medical, Inc. with the FDA for Set, Intravascular.
| Device ID | K881975 |
| 510k Number | K881975 |
| Device Name: | SET, INTRAVASCULAR |
| Classification | Set, Administration, Intravascular |
| Applicant | PRIMROSE MEDICAL, INC. 20 CABOT RD. Woburn, MA 01801 |
| Contact | Fletcher Longley |
| Correspondent | Fletcher Longley PRIMROSE MEDICAL, INC. 20 CABOT RD. Woburn, MA 01801 |
| Product Code | FPA |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-05-11 |
| Decision Date | 1988-07-29 |