ENRAF NONIVS2 CHANNEL EMG/TEMP. FEED— 510(k) K832122

Name: FDA 510(k) clearance K832122
Creator: U.S. Food and Drug Administration
Published: 1983-08-12

Substantially Equivalent

Fluidotherapy Corp.

FDA 510(k) clearance K832122 for ENRAF NONIVS2 CHANNEL EMG/TEMP. FEED, Substantially Equivalent on 1983-08-12. Applicant: Fluidotherapy Corp.. Device class: 2.

Clearance details

Applicant: Fluidotherapy Corp.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1983-06-30
Decision date: 1983-08-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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