NEUROMUSCULAR STIMULATOR— 510(k) K932611

Name: FDA 510(k) clearance K932611
Creator: U.S. Food and Drug Administration
Published: 1994-01-31

Substantially Equivalent

Myo/Kinetic Systems, Inc.

FDA 510(k) clearance K932611 for NEUROMUSCULAR STIMULATOR, Substantially Equivalent on 1994-01-31. Applicant: Myo/Kinetic Systems, Inc.. Device class: 2.

Clearance details

Applicant: Myo/Kinetic Systems, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1993-05-28
Decision date: 1994-01-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Menomonee Falls, WI, US

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