EMG BIOFEEDBACK DEVICE— 510(k) K823511

Substantially Equivalent

Nemectron Medical, Inc.

FDA 510(k) clearance K823511 for EMG BIOFEEDBACK DEVICE, Substantially Equivalent on 1983-03-31. Applicant: Nemectron Medical, Inc..

Clearance details

Applicant: Nemectron Medical, Inc.
Product code: Code HCC
Advisory panel: Neurology
Date received: 1982-11-29
Decision date: 1983-03-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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