GSA GENITO SENSORY ANALYZER— 510(k) K010981

Name: FDA 510(k) clearance K010981
Creator: U.S. Food and Drug Administration
Published: 2001-09-20

Substantially Equivalent

Medoc Ltd. Advanced Medical Systems

FDA 510(k) clearance K010981 for GSA GENITO SENSORY ANALYZER, Substantially Equivalent on 2001-09-20. Applicant: Medoc Ltd. Advanced Medical Systems. Device class: 1.

Clearance details

Applicant: Medoc Ltd. Advanced Medical Systems
Product code: Code LLN
Device class: Class 1
Regulation: 21 CFR 882.1200
Advisory panel: Neurology
Date received: 2001-04-02
Decision date: 2001-09-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minnetonka, MN, US

Download summary PDF View on FDA.gov ↗

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