ELECTRODE, NEEDLE, CFM— 510(k) K781311

Name: FDA 510(k) clearance K781311
Creator: U.S. Food and Drug Administration
Published: 1978-08-21

Substantially Equivalent

Applied Medical Research

FDA 510(k) clearance K781311 for ELECTRODE, NEEDLE, CFM, Substantially Equivalent on 1978-08-21. Applicant: Applied Medical Research. Device class: 2.

Clearance details

Applicant: Applied Medical Research
Product code: Code GXZ
Device class: Class 2
Regulation: 21 CFR 882.1350
Advisory panel: Neurology
Date received: 1978-07-31
Decision date: 1978-08-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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