The following data is part of a premarket notification filed by Ferguson Medical with the FDA for Uvp Volumed 2001.
| Device ID | K881079 |
| 510k Number | K881079 |
| Device Name: | UVP VOLUMED 2001 |
| Classification | Pump, Infusion |
| Applicant | FERGUSON MEDICAL 3407 BAY AVE. Chico, CA 95973 -8619 |
| Contact | Frank Ferguson |
| Correspondent | Frank Ferguson FERGUSON MEDICAL 3407 BAY AVE. Chico, CA 95973 -8619 |
| Product Code | FRN |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-03-14 |
| Decision Date | 1988-10-25 |