NEUROGAR III-TRANSCUT. ELEC. NERVE STIM— 510(k) K801576

Name: FDA 510(k) clearance K801576
Creator: U.S. Food and Drug Administration
Published: 1980-08-14

Substantially Equivalent

Inter Med Industries, Inc.

FDA 510(k) clearance K801576 for NEUROGAR III-TRANSCUT. ELEC. NERVE STIM, Substantially Equivalent on 1980-08-14. Applicant: Inter Med Industries, Inc.. Device class: 2.

Clearance details

Applicant: Inter Med Industries, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1980-07-09
Decision date: 1980-08-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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