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FDA 510(k)

TAPE, ELASTOPLAST ELASTIC TEAR

K-Number: K781931 · 1978-12-07

ApplicantBeiersdorf, Inc.
Decision Date1978-12-07
Product CodeFQM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TAPE, ELASTOPLAST ELASTIC TEAR is the device name listed in this FDA 510(k) record. The listed applicant is Beiersdorf, Inc.. It received FDA 510(k) clearance on 1978-12-07 under 510(k) number K781931. The device is classified under product code FQM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAPE, ELASTOPLAST ELASTIC TEAR?

TAPE, ELASTOPLAST ELASTIC TEAR is a medical device that received FDA 510(k) clearance on 1978-12-07. The listed applicant is Beiersdorf, Inc.. The 510(k) number is K781931.

When did TAPE, ELASTOPLAST ELASTIC TEAR receive FDA 510(k) clearance?

TAPE, ELASTOPLAST ELASTIC TEAR received FDA 510(k) clearance on 1978-12-07, under 510(k) number K781931.

Who is the listed applicant for TAPE, ELASTOPLAST ELASTIC TEAR?

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 TAPE, ELASTOPLAST ELASTIC TEAR?

The FDA product code for TAPE, ELASTOPLAST ELASTIC TEAR is FQM.

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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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