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FDA 510(k)

FINGER COTS

K-Number: K821028 · 1982-04-26

ApplicantAbco Dealers, Inc.
Decision Date1982-04-26
Product CodeFMC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FINGER COTS 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 1982-04-26 under 510(k) number K821028. The device is classified under product code FMC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FINGER COTS?

FINGER COTS is a medical device that received FDA 510(k) clearance on 1982-04-26. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K821028.

When did FINGER COTS receive FDA 510(k) clearance?

FINGER COTS received FDA 510(k) clearance on 1982-04-26, under 510(k) number K821028.

Who is the listed applicant for FINGER COTS?

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 FINGER COTS?

The FDA product code for FINGER COTS is FMC.

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Other records listing Abco Dealers, Inc. as applicant

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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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