ELECTRODE, MODEL E7504 PREP II

Electrosurgical, Cutting & Coagulation & Accessories

VALLEYLAB, INC.

The following data is part of a premarket notification filed by Valleylab, Inc. with the FDA for Electrode, Model E7504 Prep Ii.

Pre-market Notification Details

Device IDK790296
510k NumberK790296
Device Name:ELECTRODE, MODEL E7504 PREP II
ClassificationElectrosurgical, Cutting & Coagulation & Accessories
Applicant VALLEYLAB, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeGEI  
CFR Regulation Number878.4400 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1979-02-09
Decision Date1979-04-12

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