The following data is part of a premarket notification filed by Valleylab, Inc. with the FDA for Valleylab Model Iv7200 Infusion Pump.
| Device ID | K873161 |
| 510k Number | K873161 |
| Device Name: | VALLEYLAB MODEL IV7200 INFUSION PUMP |
| Classification | Pump, Infusion |
| Applicant | VALLEYLAB, INC. 5920 LONGBOW DR. Boulder, CO 80301 |
| Contact | Peggy Walline |
| Correspondent | Peggy Walline VALLEYLAB, INC. 5920 LONGBOW DR. Boulder, CO 80301 |
| Product Code | FRN |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-08-11 |
| Decision Date | 1987-11-05 |