CV720-727-000, MICROTIP AND FLUE PAK

Instrument, Ultrasonic Surgical

VALLEYLAB, INC.

The following data is part of a premarket notification filed by Valleylab, Inc. with the FDA for Cv720-727-000, Microtip And Flue Pak.

Pre-market Notification Details

Device IDK933239
510k NumberK933239
Device Name:CV720-727-000, MICROTIP AND FLUE PAK
ClassificationInstrument, Ultrasonic Surgical
Applicant VALLEYLAB, INC. 5920 LONGBOW DR. Boulder,  CO  80301
ContactLynne Leonard
CorrespondentLynne Leonard
VALLEYLAB, INC. 5920 LONGBOW DR. Boulder,  CO  80301
Product CodeLFL  
CFR Regulation Number510(k) Premarket Notification [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1993-07-02
Decision Date1993-10-12

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