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

Name: FDA 510(k) clearance K961050
Creator: U.S. Food and Drug Administration
Published: 1997-08-01

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.. Device class: 2.

Clearance details

Applicant: Maven Labs, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1996-02-08
Decision date: 1997-08-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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