FDA 510(k)

CONMED ANDOVER MED ECG ELECTRODES

K-Number: K942925 · 1994-07-20

Decision Date1994-07-20

Product CodeDRX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CONMED ANDOVER MED ECG ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Conmed Andover Medical, Inc.. It received FDA 510(k) clearance on 1994-07-20 under 510(k) number K942925. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONMED ANDOVER MED ECG ELECTRODES?

CONMED ANDOVER MED ECG ELECTRODES is a medical device that received FDA 510(k) clearance on 1994-07-20. The listed applicant is Conmed Andover Medical, Inc.. The 510(k) number is K942925.

When did CONMED ANDOVER MED ECG ELECTRODES receive FDA 510(k) clearance?

CONMED ANDOVER MED ECG ELECTRODES received FDA 510(k) clearance on 1994-07-20, under 510(k) number K942925.

Who is the listed applicant for CONMED ANDOVER MED ECG ELECTRODES?

The FDA 510(k) record lists Conmed Andover Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONMED ANDOVER MED ECG ELECTRODES?

The FDA product code for CONMED ANDOVER MED ECG ELECTRODES is DRX.

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Other records listing Conmed Andover Medical, Inc. as applicant

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Related Devices (Code: DRX)

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Official Source

View on FDA Database →

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