ELECTRO-NEVE STIMULATOR TENS MODEL BIOMED PLUS/A— 510(k) K905230

Name: FDA 510(k) clearance K905230
Creator: U.S. Food and Drug Administration
Published: 1991-06-04

Substantially Equivalent

Biomedical Life Systems, Inc.

FDA 510(k) clearance K905230 for ELECTRO-NEVE STIMULATOR TENS MODEL BIOMED PLUS/A, Substantially Equivalent on 1991-06-04. 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: 1990-11-20
Decision date: 1991-06-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Marcos, CA, US

Download summary PDF View on FDA.gov ↗

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