MYO-ACTUATOR— 510(k) K852963

Substantially Equivalent

Verimed Holdings, Inc.

FDA 510(k) clearance K852963 for MYO-ACTUATOR, Substantially Equivalent on 1986-01-21. Applicant: Verimed Holdings, Inc..

Clearance details

Applicant: Verimed Holdings, Inc.
Product code: Code HCC
Advisory panel: Neurology
Date received: 1985-07-12
Decision date: 1986-01-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Lauderdale, FL, US

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