The following data is part of a premarket notification filed by Marquette Medical, Inc. with the FDA for Pump Tubing Set.
| Device ID | K873495 |
| 510k Number | K873495 |
| Device Name: | PUMP TUBING SET |
| Classification | Pump, Infusion |
| Applicant | MARQUETTE MEDICAL, INC. 2134 ESPEY CT. #7 Crofton, MD 21114 |
| Contact | Earl D Marquette |
| Correspondent | Earl D Marquette MARQUETTE MEDICAL, INC. 2134 ESPEY CT. #7 Crofton, MD 21114 |
| Product Code | FRN |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-08-31 |
| Decision Date | 1987-12-30 |