The following data is part of a premarket notification filed by 3m Health Care, Ltd. with the FDA for Avi Model 3000 Infusion Pump.
| Device ID | K920588 |
| 510k Number | K920588 |
| Device Name: | AVI MODEL 3000 INFUSION PUMP |
| Classification | Pump, Infusion |
| Applicant | 3M HEALTH CARE, LTD. 3M CENTER, BLDG. 275-3E-08 P.O. BOX 33275 St. Paul, MN 55133 |
| Contact | Stanley J Suedkamp |
| Correspondent | Stanley J Suedkamp 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 | 1992-02-10 |
| Decision Date | 1992-04-06 |