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FDA 510(k)

TRIANGULAR BANDAGE

K-Number: K811814 · 1981-07-31

ApplicantAbco Dealers, Inc.
Decision Date1981-07-31
Product CodeNAB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TRIANGULAR BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is Abco Dealers, Inc.. It received FDA 510(k) clearance on 1981-07-31 under 510(k) number K811814. The device is classified under product code NAB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIANGULAR BANDAGE?

TRIANGULAR BANDAGE is a medical device that received FDA 510(k) clearance on 1981-07-31. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K811814.

When did TRIANGULAR BANDAGE receive FDA 510(k) clearance?

TRIANGULAR BANDAGE received FDA 510(k) clearance on 1981-07-31, under 510(k) number K811814.

Who is the listed applicant for TRIANGULAR BANDAGE?

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

What is the FDA product code for TRIANGULAR BANDAGE?

The FDA product code for TRIANGULAR BANDAGE is NAB.

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Other records listing Abco Dealers, Inc. as applicant

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Related Devices (Code: NAB)

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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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