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FDA 510(k)

XYLOS XCELL ANTIMICROBIAL DRESSING

K-Number: K024054 · 2003-03-07

Decision Date2003-03-07
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

XYLOS XCELL ANTIMICROBIAL DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Xylos Corporation. It received FDA 510(k) clearance on 2003-03-07 under 510(k) number K024054. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XYLOS XCELL ANTIMICROBIAL DRESSING?

XYLOS XCELL ANTIMICROBIAL DRESSING is a medical device that received FDA 510(k) clearance on 2003-03-07. The listed applicant is Xylos Corporation. The 510(k) number is K024054.

When did XYLOS XCELL ANTIMICROBIAL DRESSING receive FDA 510(k) clearance?

XYLOS XCELL ANTIMICROBIAL DRESSING received FDA 510(k) clearance on 2003-03-07, under 510(k) number K024054.

Who is the listed applicant for XYLOS XCELL ANTIMICROBIAL DRESSING?

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

What is the FDA product code for XYLOS XCELL ANTIMICROBIAL DRESSING?

The FDA product code for XYLOS XCELL ANTIMICROBIAL DRESSING is MGQ.

Related Clinical Trials

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.

Other records listing Xylos Corporation as applicant

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.

View all 9 devices →

Related Devices (Code: MGQ)

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.

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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