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FDA 510(k)

LYOCELL WOUND DRESSING/SURGICAL SPONGE

K-Number: K972458 · 1997-09-19

Decision Date1997-09-19
Product CodeMGP
DecisionSubstantially Equivalent

Device Summary

LYOCELL WOUND DRESSING/SURGICAL SPONGE is the device name listed in this FDA 510(k) record. The listed applicant is Courtaulds Fibers, Inc.. It received FDA 510(k) clearance on 1997-09-19 under 510(k) number K972458. The device is classified under product code MGP. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LYOCELL WOUND DRESSING/SURGICAL SPONGE?

LYOCELL WOUND DRESSING/SURGICAL SPONGE is a medical device that received FDA 510(k) clearance on 1997-09-19. The listed applicant is Courtaulds Fibers, Inc.. The 510(k) number is K972458.

When did LYOCELL WOUND DRESSING/SURGICAL SPONGE receive FDA 510(k) clearance?

LYOCELL WOUND DRESSING/SURGICAL SPONGE received FDA 510(k) clearance on 1997-09-19, under 510(k) number K972458.

Who is the listed applicant for LYOCELL WOUND DRESSING/SURGICAL SPONGE?

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

What is the FDA product code for LYOCELL WOUND DRESSING/SURGICAL SPONGE?

The FDA product code for LYOCELL WOUND DRESSING/SURGICAL SPONGE is MGP.

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 Courtaulds Fibers, Inc. 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.

Related Devices (Code: MGP)

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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