The following data is part of a premarket notification filed by Valleylab, Inc. with the FDA for Iv7200 And Iv7400 Infusion Pump.
Device ID | K860694 |
510k Number | K860694 |
Device Name: | IV7200 AND IV7400 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 | 1986-02-25 |
Decision Date | 1986-04-22 |