M AND R REUSABLE ELECTRODES (MULTIPLE)— 510(k) K963125

Name: FDA 510(k) clearance K963125
Creator: U.S. Food and Drug Administration
Published: 1997-02-06

Substantially Equivalent

M & R Mfg., Inc.

FDA 510(k) clearance K963125 for M AND R REUSABLE ELECTRODES (MULTIPLE), Substantially Equivalent on 1997-02-06. Applicant: M & R Mfg., Inc.. Device class: 2.

Clearance details

Applicant: M & R Mfg., Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1996-08-12
Decision date: 1997-02-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fredericktown, OH, US

Download summary PDF View on FDA.gov ↗

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