SOKEN PLUS(TM) ELECTRONIC MUSCLE STIMULATOR— 510(k) K881470

Name: FDA 510(k) clearance K881470
Creator: U.S. Food and Drug Administration
Published: 1989-03-10

Substantially Equivalent

Rehab Medical Specialties, Inc.

FDA 510(k) clearance K881470 for SOKEN PLUS(TM) ELECTRONIC MUSCLE STIMULATOR, Substantially Equivalent on 1989-03-10. Applicant: Rehab Medical Specialties, Inc.. Device class: 2.

Clearance details

Applicant: Rehab Medical Specialties, Inc.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1988-04-07
Decision date: 1989-03-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Garland, TX, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.