MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC— 510(k) K902976

Name: FDA 510(k) clearance K902976
Creator: U.S. Food and Drug Administration
Published: 1990-09-07

Substantially Equivalent

Medical Consultants Intl. , Ltd.

FDA 510(k) clearance K902976 for MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC, Substantially Equivalent on 1990-09-07. Applicant: Medical Consultants Intl. , Ltd.. Device class: 2.

Clearance details

Applicant: Medical Consultants Intl. , Ltd.
Product code: Code GZL
Device class: Class 2
Regulation: 21 CFR 882.1330
Advisory panel: Neurology
Date received: 1990-07-06
Decision date: 1990-09-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Glen Rock, NJ, US

Download summary PDF View on FDA.gov ↗

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