The following data is part of a premarket notification filed by Marquette Medical, Inc. with the FDA for Marquette Medical, Inc. Iv Extension Sets.
| Device ID | K880928 |
| 510k Number | K880928 |
| Device Name: | MARQUETTE MEDICAL, INC. IV EXTENSION SETS |
| Classification | Set, Administration, Intravascular |
| Applicant | MARQUETTE MEDICAL, INC. 2134 ESPEY CT. #7 Crofton, MD 21114 |
| Contact | Marquette Jr |
| Correspondent | Marquette Jr MARQUETTE MEDICAL, INC. 2134 ESPEY CT. #7 Crofton, MD 21114 |
| Product Code | FPA |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-03-04 |
| Decision Date | 1988-04-29 |