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FDA 510(k)

LEUKOSILK(TM) SURGICAL TAPE

K-Number: K896891 · 1990-02-09

Decision Date1990-02-09
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LEUKOSILK(TM) SURGICAL TAPE is the device name listed in this FDA 510(k) record. The listed applicant is Beiersdorf, Inc.. It received FDA 510(k) clearance on 1990-02-09 under 510(k) number K896891. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEUKOSILK(TM) SURGICAL TAPE?

LEUKOSILK(TM) SURGICAL TAPE is a medical device that received FDA 510(k) clearance on 1990-02-09. The listed applicant is Beiersdorf, Inc.. The 510(k) number is K896891.

When did LEUKOSILK(TM) SURGICAL TAPE receive FDA 510(k) clearance?

LEUKOSILK(TM) SURGICAL TAPE received FDA 510(k) clearance on 1990-02-09, under 510(k) number K896891.

Who is the listed applicant for LEUKOSILK(TM) SURGICAL TAPE?

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

What is the FDA product code for LEUKOSILK(TM) SURGICAL TAPE?

The FDA product code for LEUKOSILK(TM) SURGICAL TAPE is KGX.

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 Beiersdorf, 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 45 devices →

Related Devices (Code: KGX)

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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