IV7200 AND IV7400 INFUSION PUMP

Pump, Infusion

VALLEYLAB, INC.

The following data is part of a premarket notification filed by Valleylab, Inc. with the FDA for Iv7200 And Iv7400 Infusion Pump.

Pre-market Notification Details

Device IDK860694
510k NumberK860694
Device Name:IV7200 AND IV7400 INFUSION PUMP
ClassificationPump, Infusion
Applicant VALLEYLAB, INC. 5920 LONGBOW DR. Boulder,  CO  80301
ContactPeggy Walline
CorrespondentPeggy Walline
VALLEYLAB, INC. 5920 LONGBOW DR. Boulder,  CO  80301
Product CodeFRN  
CFR Regulation Number880.5725 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1986-02-25
Decision Date1986-04-22

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.