Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LEUKOPOR(TM) SURGICAL TAPE

K-Number: K881509 · 1988-04-22

Decision Date1988-04-22
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LEUKOPOR(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 1988-04-22 under 510(k) number K881509. 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 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.

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑