The following data is part of a premarket notification filed by I-flow Corp. with the FDA for Vivus 5000 Infusion System.
| Device ID | K924527 |
| 510k Number | K924527 |
| Device Name: | VIVUS 5000 INFUSION SYSTEM |
| Classification | Pump, Infusion |
| Applicant | I-FLOW CORP. 2532 WHITE RD. Irvine, CA 92714 |
| Contact | Robert J Bard |
| Correspondent | Robert J Bard I-FLOW CORP. 2532 WHITE RD. Irvine, CA 92714 |
| Product Code | FRN |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-09-08 |
| Decision Date | 1994-03-29 |