RELIEF BAND (T.E.N.S. DEVICE)— 510(k) K901704

Substantially Equivalent

Maven Labs, Inc.

FDA 510(k) clearance K901704 for RELIEF BAND (T.E.N.S. DEVICE), Substantially Equivalent on 1991-11-19. 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: 1990-04-12
Decision date: 1991-11-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sacramento, CA, US

Download summary PDF View on FDA.gov ↗

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