MODEL SSE4 ELECTROSURGICAL GENERATOR

Electrosurgical, Cutting & Coagulation & Accessories

VALLEYLAB, INC.

The following data is part of a premarket notification filed by Valleylab, Inc. with the FDA for Model Sse4 Electrosurgical Generator.

Pre-market Notification Details

Device IDK823924
510k NumberK823924
Device Name:MODEL SSE4 ELECTROSURGICAL GENERATOR
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 Received1982-12-28
Decision Date1983-01-09

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