LEUKOPOR(TM) SURGICAL TAPE
K-Number: K881509 · 1988-04-22
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Device Summary
Frequently Asked Questions
What is the LEUKOPOR(TM) SURGICAL TAPE?
LEUKOPOR(TM) SURGICAL TAPE is a medical device that received FDA 510(k) clearance on 1988-04-22. The listed applicant is Beiersdorf, Inc.. The 510(k) number is K881509.
When did LEUKOPOR(TM) SURGICAL TAPE receive FDA 510(k) clearance?
LEUKOPOR(TM) SURGICAL TAPE received FDA 510(k) clearance on 1988-04-22, under 510(k) number K881509.
Who is the listed applicant for LEUKOPOR(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 LEUKOPOR(TM) SURGICAL TAPE?
The FDA product code for LEUKOPOR(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.
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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