ELECTRO-NERVE STIMULATOR TENS MODEL BMLS02-3— 510(k) K021271

Name: FDA 510(k) clearance K021271
Creator: U.S. Food and Drug Administration
Published: 2003-02-06

Substantially Equivalent

Biomedical Life Systems

FDA 510(k) clearance K021271 for ELECTRO-NERVE STIMULATOR TENS MODEL BMLS02-3, Substantially Equivalent on 2003-02-06. Applicant: Biomedical Life Systems. Device class: 2.

Clearance details

Applicant: Biomedical Life Systems
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2002-04-22
Decision date: 2003-02-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Vista, CA, US

Download summary PDF View on FDA.gov ↗

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