The following data is part of a premarket notification filed by 3m Health Care, Ltd. with the FDA for Avi Model 600 Syringe Pump.
| Device ID | K933005 |
| 510k Number | K933005 |
| Device Name: | AVI MODEL 600 SYRINGE PUMP |
| Classification | Pump, Infusion |
| Applicant | 3M HEALTH CARE, LTD. 3M CENTER, BLDG. 275-3E-08 P.O. BOX 33275 St. Paul, MN 55133 |
| Contact | Von Busch |
| Correspondent | Von Busch 3M HEALTH CARE, LTD. 3M CENTER, BLDG. 275-3E-08 P.O. BOX 33275 St. Paul, MN 55133 |
| Product Code | FRN |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-06-21 |
| Decision Date | 1993-10-25 |