LECTROSWITCH MODEL E2502B

Electrosurgical, Cutting & Coagulation & Accessories

VALLEYLAB, INC.

The following data is part of a premarket notification filed by Valleylab, Inc. with the FDA for Lectroswitch Model E2502b.

Pre-market Notification Details

Device IDK781511
510k NumberK781511
Device Name:LECTROSWITCH MODEL E2502B
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 Received1978-09-01
Decision Date1978-10-24

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
10884521175662 K781511 000

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