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FDA 510(k)

X-CELL WOUND DRESSING

K-Number: K974251 · 1998-06-22

ApplicantXylos Corporation
Decision Date1998-06-22
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

X-CELL WOUND 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 1998-06-22 under 510(k) number K974251. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X-CELL WOUND DRESSING?

X-CELL WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1998-06-22. The listed applicant is Xylos Corporation. The 510(k) number is K974251.

When did X-CELL WOUND DRESSING receive FDA 510(k) clearance?

X-CELL WOUND DRESSING received FDA 510(k) clearance on 1998-06-22, under 510(k) number K974251.

Who is the listed applicant for X-CELL WOUND 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 X-CELL WOUND DRESSING?

The FDA product code for X-CELL WOUND DRESSING is MGQ.

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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.

K111584XYLOS MACRO-POROUS SURGICAL MESHK100984XYLOS VESSEL GUARDK090880XYLOS POROUS SURGICAL MESHK090778MTA PROTECTIVE SHEETK083823SECURIAN TISSUE REINFORCEMENT MATRIXK081882MODIFICATION TO XYLOS SURGICAL MESH

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Related Devices (Code: MGQ)

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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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