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FDA 510(k)

LEUKOFIX POROS

K-Number: K792726 · 1980-02-28

ApplicantBeiersdorf, Inc.
Decision Date1980-02-28
Product CodeFPX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LEUKOFIX POROS is the device name listed in this FDA 510(k) record. The listed applicant is Beiersdorf, Inc.. It received FDA 510(k) clearance on 1980-02-28 under 510(k) number K792726. The device is classified under product code FPX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEUKOFIX POROS?

LEUKOFIX POROS is a medical device that received FDA 510(k) clearance on 1980-02-28. The listed applicant is Beiersdorf, Inc.. The 510(k) number is K792726.

When did LEUKOFIX POROS receive FDA 510(k) clearance?

LEUKOFIX POROS received FDA 510(k) clearance on 1980-02-28, under 510(k) number K792726.

Who is the listed applicant for LEUKOFIX POROS?

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 LEUKOFIX POROS?

The FDA product code for LEUKOFIX POROS is FPX.

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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.

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Related Devices (Code: FPX)

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.

K970441K-KLOSURE 2 INCH LENGTH/4 INCH LENGTH/8 INCH LENGTH/12 INCH LENGTHMedi-Flex Hospital Products, Inc.K952947DELPORE SKIN CLOSUREBitco Intl.K952702DERMA SEALTtl MedicalK946321BIOSTRIP STERILE WOUND CLOSURE STRIPCornelia Damsky, Inc.K931005DUKAL SKIN CLOSURE STRIPDukal Corp.K921775SPYROFLEX WOUND CLOSURESPolymint Industrial Co. , Ltd.

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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