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FDA 510(k)

HYDRON BURN BANDAGE MANUAL APPLICATION

K-Number: K781406 · 1978-09-07

ApplicantAbbott Laboratories
Decision Date1978-09-07
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HYDRON BURN BANDAGE MANUAL APPLICATION is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1978-09-07 under 510(k) number K781406. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYDRON BURN BANDAGE MANUAL APPLICATION?

HYDRON BURN BANDAGE MANUAL APPLICATION is a medical device that received FDA 510(k) clearance on 1978-09-07. The listed applicant is Abbott Laboratories. The 510(k) number is K781406.

When did HYDRON BURN BANDAGE MANUAL APPLICATION receive FDA 510(k) clearance?

HYDRON BURN BANDAGE MANUAL APPLICATION received FDA 510(k) clearance on 1978-09-07, under 510(k) number K781406.

Who is the listed applicant for HYDRON BURN BANDAGE MANUAL APPLICATION?

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

What is the FDA product code for HYDRON BURN BANDAGE MANUAL APPLICATION?

The FDA product code for HYDRON BURN BANDAGE MANUAL APPLICATION is KMF.

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Related Devices (Code: KMF)

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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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