AD-TECH SUB DURAL ELECTRODEDS— 510(k) K923803

Substantially Equivalent

Ad-Tech Medical Instrument Corp

FDA 510(k) clearance K923803 for AD-TECH SUB DURAL ELECTRODEDS, Substantially Equivalent on 1992-10-23. Applicant: Ad-Tech Medical Instrument Corp.

Clearance details

Applicant: Ad-Tech Medical Instrument Corp
Product code: Code GYC
Advisory panel: Neurology
Date received: 1992-07-29
Decision date: 1992-10-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Racine, WI, US

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