LEUKOSPORT(TM) ADHESIVE TAPE
K-Number: K894367 · 1989-11-15
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Device Summary
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.
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
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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