THERAPEUTIC STIM 200 (TS-200)/200P (TS-200P)— 510(k) K932399

Name: FDA 510(k) clearance K932399
Creator: U.S. Food and Drug Administration
Published: 1993-08-11

Substantially Equivalent

Myo/Kinetic Systems, Inc.

FDA 510(k) clearance K932399 for THERAPEUTIC STIM 200 (TS-200)/200P (TS-200P), Substantially Equivalent on 1993-08-11. Applicant: Myo/Kinetic Systems, Inc.. Device class: 2.

Clearance details

Applicant: Myo/Kinetic Systems, Inc.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1993-05-18
Decision date: 1993-08-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Menomonee Falls, WI, US

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