STIMULATOR, ELECTRICAL MUSCLE (#MD-8)— 510(k) K760503

Name: FDA 510(k) clearance K760503
Creator: U.S. Food and Drug Administration
Published: 1976-09-27

Substantially Equivalent

R. A. Fischer Co. Corp.

FDA 510(k) clearance K760503 for STIMULATOR, ELECTRICAL MUSCLE (#MD-8), Substantially Equivalent on 1976-09-27. Applicant: R. A. Fischer Co. Corp.. Device class: 2.

Clearance details

Applicant: R. A. Fischer Co. Corp.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1976-08-23
Decision date: 1976-09-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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