MYOMETER EMG BIOFEEDBACK DEVICE— 510(k) K850849

Substantially Equivalent

Physio Technology, Inc.

FDA 510(k) clearance K850849 for MYOMETER EMG BIOFEEDBACK DEVICE, Substantially Equivalent on 1985-05-31. Applicant: Physio Technology, Inc..

Clearance details

Applicant: Physio Technology, Inc.
Product code: Code HCC
Advisory panel: Neurology
Date received: 1985-03-01
Decision date: 1985-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Topeka, KS, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.