FDA 510(k)

M AND R REUSABLE ELECTRODES (MULTIPLE)

K-Number: K963125 · 1997-02-06

Decision Date1997-02-06

Product CodeGZJ

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

M AND R REUSABLE ELECTRODES (MULTIPLE) is the device name listed in this FDA 510(k) record. The listed applicant is M & R Mfg., Inc.. It received FDA 510(k) clearance on 1997-02-06 under 510(k) number K963125. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the M AND R REUSABLE ELECTRODES (MULTIPLE)?

M AND R REUSABLE ELECTRODES (MULTIPLE) is a medical device that received FDA 510(k) clearance on 1997-02-06. The listed applicant is M & R Mfg., Inc.. The 510(k) number is K963125.

When did M AND R REUSABLE ELECTRODES (MULTIPLE) receive FDA 510(k) clearance?

M AND R REUSABLE ELECTRODES (MULTIPLE) received FDA 510(k) clearance on 1997-02-06, under 510(k) number K963125.

Who is the listed applicant for M AND R REUSABLE ELECTRODES (MULTIPLE)?

The FDA 510(k) record lists M & R Mfg., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for M AND R REUSABLE ELECTRODES (MULTIPLE)?

The FDA product code for M AND R REUSABLE ELECTRODES (MULTIPLE) is GZJ.

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Other records listing M & R Mfg., Inc. as applicant

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Related Devices (Code: GZJ)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.