LB-2000 CRANIAL ELECTROTHERAPY STIMULATOR— 510(k) K910616

Name: FDA 510(k) clearance K910616
Creator: U.S. Food and Drug Administration
Published: 1992-05-12

Substantially Equivalent

Life Balance Intl., Inc.

FDA 510(k) clearance K910616 for LB-2000 CRANIAL ELECTROTHERAPY STIMULATOR, Substantially Equivalent on 1992-05-12. Applicant: Life Balance Intl., Inc.. Device class: 2.

Clearance details

Applicant: Life Balance Intl., Inc.
Product code: Code QJQ
Device class: Class 2
Regulation: 21 CFR 882.5800
Advisory panel: Neurology
Date received: 1991-02-12
Decision date: 1992-05-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: East Draper, UT, US

Download summary PDF View on FDA.gov ↗

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