NEUROGAR III— 510(k) K812036

Substantially Equivalent

Inter Med Industries, Inc.

FDA 510(k) clearance K812036 for NEUROGAR III, Substantially Equivalent on 1981-08-07. 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: 1981-07-20
Decision date: 1981-08-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Inter Med Industries, Inc.

K801577 — NEUROGAR IV-EXTERNAL NEURO-MUSCLE STIM.1980-08-27
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Data sourced from openFDA. This site is unofficial and independent of the FDA.