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FDA 510(k)

SIS WOUND DRESSING

K-Number: K973170 · 1998-04-30

Decision Date1998-04-30
Product CodeKGN
DecisionSubstantially Equivalent

Device Summary

SIS WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Cook Biotech, Inc.. It received FDA 510(k) clearance on 1998-04-30 under 510(k) number K973170. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIS WOUND DRESSING?

SIS WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1998-04-30. The listed applicant is Cook Biotech, Inc.. The 510(k) number is K973170.

When did SIS WOUND DRESSING receive FDA 510(k) clearance?

SIS WOUND DRESSING received FDA 510(k) clearance on 1998-04-30, under 510(k) number K973170.

Who is the listed applicant for SIS WOUND DRESSING?

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

What is the FDA product code for SIS WOUND DRESSING?

The FDA product code for SIS WOUND DRESSING is KGN.

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 Cook Biotech, 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.

View all 29 devices →

Related Devices (Code: KGN)

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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