KINESTIM MUSCLE STIMULATOR— 510(k) K871472

Name: FDA 510(k) clearance K871472
Creator: U.S. Food and Drug Administration
Published: 1987-06-29

Substantially Equivalent for Some Indications

Promatek Industries, Ltd.

FDA 510(k) clearance K871472 for KINESTIM MUSCLE STIMULATOR, Substantially Equivalent for Some Indications on 1987-06-29. Applicant: Promatek Industries, Ltd.. Device class: 2.

Clearance details

Applicant: Promatek Industries, Ltd.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1987-04-14
Decision date: 1987-06-29
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Quebec, H4p 2c9, CA

Download summary PDF View on FDA.gov ↗

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