The following data is part of a premarket notification filed by 3m Company with the FDA for Model 280 Infusion Pump.
| Device ID | K894360 |
| 510k Number | K894360 |
| Device Name: | MODEL 280 INFUSION PUMP |
| Classification | Pump, Infusion |
| Applicant | 3M COMPANY 1120 RED FOX RD. St. Paul, MN 55112 |
| Contact | Von Busch |
| Correspondent | Von Busch 3M COMPANY 1120 RED FOX RD. St. Paul, MN 55112 |
| Product Code | FRN |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-07-14 |
| Decision Date | 1989-10-04 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 30610586100509 | K894360 | 000 |
| 30610586100486 | K894360 | 000 |
| 30610586100479 | K894360 | 000 |
| 30610586100462 | K894360 | 000 |
| 30610586100196 | K894360 | 000 |
| 30610586100189 | K894360 | 000 |
| 30610586100172 | K894360 | 000 |