The following data is part of a premarket notification filed by 3m Health Care, Ltd. with the FDA for Model 480 Infusion Pump, Modification.
| Device ID | K924868 |
| 510k Number | K924868 |
| Device Name: | MODEL 480 INFUSION PUMP, MODIFICATION |
| Classification | Pump, Infusion |
| Applicant | 3M HEALTH CARE, LTD. 3M CENTER, BLDG. 275-3E-08 P.O. BOX 33275 St. Paul, MN 55133 |
| Contact | Stan Suedkamp |
| Correspondent | Stan 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 | 1992-09-23 |
| Decision Date | 1993-06-17 |