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FDA 510(k)

FIXOMULL STERILE

K-Number: K800953 · 1980-05-20

ApplicantBeiersdorf, Inc.
Decision Date1980-05-20
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FIXOMULL STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Beiersdorf, Inc.. It received FDA 510(k) clearance on 1980-05-20 under 510(k) number K800953. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIXOMULL STERILE?

FIXOMULL STERILE is a medical device that received FDA 510(k) clearance on 1980-05-20. The listed applicant is Beiersdorf, Inc.. The 510(k) number is K800953.

When did FIXOMULL STERILE receive FDA 510(k) clearance?

FIXOMULL STERILE received FDA 510(k) clearance on 1980-05-20, under 510(k) number K800953.

Who is the listed applicant for FIXOMULL STERILE?

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 FIXOMULL STERILE?

The FDA product code for FIXOMULL STERILE is NAD.

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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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