ELECTRO-NERVE STIMULATOR TENS MODEL MICRO PLUS-A— 510(k) K915210

Name: FDA 510(k) clearance K915210
Creator: U.S. Food and Drug Administration
Published: 1992-05-04

Substantially Equivalent

Biomedical Life Systems, Inc.

FDA 510(k) clearance K915210 for ELECTRO-NERVE STIMULATOR TENS MODEL MICRO PLUS-A, Substantially Equivalent on 1992-05-04. Applicant: Biomedical Life Systems, Inc.. Device class: 2.

Clearance details

Applicant: Biomedical Life Systems, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1991-11-18
Decision date: 1992-05-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Vista, CA, US

Download summary PDF View on FDA.gov ↗

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