MYOTRACE 10 BIOFEEDBACK DEVICE— 510(k) K895633

Substantially Equivalent

Noraxon USA, Inc.

FDA 510(k) clearance K895633 for MYOTRACE 10 BIOFEEDBACK DEVICE, Substantially Equivalent on 1990-04-13. Applicant: Noraxon USA, Inc..

Clearance details

Applicant: Noraxon USA, Inc.
Product code: Code HCC
Advisory panel: Neurology
Date received: 1989-09-19
Decision date: 1990-04-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Scottsdale, AZ, US

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