CADWELL 7000 ELECTROMYOGRAPH MACHINE— 510(k) K791235

Name: FDA 510(k) clearance K791235
Creator: U.S. Food and Drug Administration
Published: 1979-08-16

Substantially Equivalent

Cadwell Laboratories, Inc.

FDA 510(k) clearance K791235 for CADWELL 7000 ELECTROMYOGRAPH MACHINE, Substantially Equivalent on 1979-08-16. Applicant: Cadwell Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Cadwell Laboratories, Inc.
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 1979-07-06
Decision date: 1979-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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