The following data is part of a premarket notification filed by Valleylab, Inc. with the FDA for Model Iv 6500 Formulator.
| Device ID | K792142 |
| 510k Number | K792142 |
| Device Name: | MODEL IV 6500 FORMULATOR |
| Classification | Pump, Infusion |
| Applicant | VALLEYLAB, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FRN |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-10-26 |
| Decision Date | 1979-11-29 |