RELIEFBAND TENS UNIT (MODIFICATION)— 510(k) K961050

Substantially Equivalent

Maven Labs, Inc.

FDA 510(k) clearance K961050 for RELIEFBAND TENS UNIT (MODIFICATION), Substantially Equivalent on 1997-08-01. Applicant: Maven Labs, Inc..

Clearance details

Applicant: Maven Labs, Inc.
Product code: Code GZJ
Advisory panel: Neurology
Date received: 1996-02-08
Decision date: 1997-08-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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