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FDA 510(k)

CARDIOTECH ANTIBOTIC HYDROGEL WOUND DRESSING

K-Number: K022584 · 2002-12-30

ApplicantCardiotech Intl.
Decision Date2002-12-30
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

CARDIOTECH ANTIBOTIC HYDROGEL WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Cardiotech Intl.. It received FDA 510(k) clearance on 2002-12-30 under 510(k) number K022584. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDIOTECH ANTIBOTIC HYDROGEL WOUND DRESSING?

CARDIOTECH ANTIBOTIC HYDROGEL WOUND DRESSING is a medical device that received FDA 510(k) clearance on 2002-12-30. The listed applicant is Cardiotech Intl.. The 510(k) number is K022584.

When did CARDIOTECH ANTIBOTIC HYDROGEL WOUND DRESSING receive FDA 510(k) clearance?

CARDIOTECH ANTIBOTIC HYDROGEL WOUND DRESSING received FDA 510(k) clearance on 2002-12-30, under 510(k) number K022584.

Who is the listed applicant for CARDIOTECH ANTIBOTIC HYDROGEL WOUND DRESSING?

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

What is the FDA product code for CARDIOTECH ANTIBOTIC HYDROGEL WOUND DRESSING?

The FDA product code for CARDIOTECH ANTIBOTIC HYDROGEL WOUND DRESSING is MGQ.

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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.

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