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FDA 510(k)

CONMED 2710 CLEARTRACE 2 LT MONITORING ECG ELECTRODE

K-Number: K954388 · 1996-02-06

ApplicantConmedcorp
Decision Date1996-02-06
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CONMED 2710 CLEARTRACE 2 LT MONITORING ECG ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1996-02-06 under 510(k) number K954388. 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 2710 CLEARTRACE 2 LT MONITORING ECG ELECTRODE?

CONMED 2710 CLEARTRACE 2 LT MONITORING ECG ELECTRODE is a medical device that received FDA 510(k) clearance on 1996-02-06. The listed applicant is Conmedcorp. The 510(k) number is K954388.

When did CONMED 2710 CLEARTRACE 2 LT MONITORING ECG ELECTRODE receive FDA 510(k) clearance?

CONMED 2710 CLEARTRACE 2 LT MONITORING ECG ELECTRODE received FDA 510(k) clearance on 1996-02-06, under 510(k) number K954388.

Who is the listed applicant for CONMED 2710 CLEARTRACE 2 LT MONITORING ECG ELECTRODE?

The FDA 510(k) record lists Conmedcorp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONMED 2710 CLEARTRACE 2 LT MONITORING ECG ELECTRODE?

The FDA product code for CONMED 2710 CLEARTRACE 2 LT MONITORING ECG ELECTRODE is DRX.

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Related Devices (Code: DRX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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