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FDA 510(k)

BANDAGE, ELASTIC

K-Number: K780231 · 1978-02-21

ApplicantBiomet, Inc.
Decision Date1978-02-21
Product CodeFQM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BANDAGE, ELASTIC is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 1978-02-21 under 510(k) number K780231. 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 BANDAGE, ELASTIC?

BANDAGE, ELASTIC is a medical device that received FDA 510(k) clearance on 1978-02-21. The listed applicant is Biomet, Inc.. The 510(k) number is K780231.

When did BANDAGE, ELASTIC receive FDA 510(k) clearance?

BANDAGE, ELASTIC received FDA 510(k) clearance on 1978-02-21, under 510(k) number K780231.

Who is the listed applicant for BANDAGE, ELASTIC?

The FDA 510(k) record lists Biomet, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BANDAGE, ELASTIC?

The FDA product code for BANDAGE, ELASTIC is FQM.

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Related Devices (Code: 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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