MLS ELECTROMYOGRAPHIC PREAMPLIFIER— 510(k) K974385

Name: FDA 510(k) clearance K974385
Creator: U.S. Food and Drug Administration
Published: 1998-02-19

Substantially Equivalent

Motion Lab Systems, Inc.

FDA 510(k) clearance K974385 for MLS ELECTROMYOGRAPHIC PREAMPLIFIER, Substantially Equivalent on 1998-02-19. Applicant: Motion Lab Systems, Inc.. Device class: 2.

Clearance details

Applicant: Motion Lab Systems, Inc.
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 1997-11-21
Decision date: 1998-02-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Baton Rouge, LA, US

Download summary PDF View on FDA.gov ↗

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