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FDA 510(k)

LEUKOSPORT(TM) ADHESIVE TAPE

K-Number: K894367 · 1989-11-15

Decision Date1989-11-15
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

LEUKOSPORT(TM) ADHESIVE 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 1989-11-15 under 510(k) number K894367. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the LEUKOSPORT(TM) ADHESIVE TAPE?

LEUKOSPORT(TM) ADHESIVE TAPE is a medical device that received FDA 510(k) clearance on 1989-11-15. The listed applicant is Beiersdorf, Inc.. The 510(k) number is K894367.

When did LEUKOSPORT(TM) ADHESIVE TAPE receive FDA 510(k) clearance?

LEUKOSPORT(TM) ADHESIVE TAPE received FDA 510(k) clearance on 1989-11-15, under 510(k) number K894367.

Who is the listed applicant for LEUKOSPORT(TM) ADHESIVE 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 LEUKOSPORT(TM) ADHESIVE TAPE?

The FDA product code for LEUKOSPORT(TM) ADHESIVE 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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