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FDA 510(k)

INSTRUMENT CLEANER LIQUID CONCENTRATE

K-Number: K803154 · 1981-05-11

ApplicantAbco Dealers, Inc.
Decision Date1981-05-11
Product Code
DecisionSubstantially Equivalent

Device Summary

INSTRUMENT CLEANER LIQUID CONCENTRATE 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 1981-05-11 under 510(k) number K803154. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTRUMENT CLEANER LIQUID CONCENTRATE?

INSTRUMENT CLEANER LIQUID CONCENTRATE is a medical device that received FDA 510(k) clearance on 1981-05-11. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K803154.

When did INSTRUMENT CLEANER LIQUID CONCENTRATE receive FDA 510(k) clearance?

INSTRUMENT CLEANER LIQUID CONCENTRATE received FDA 510(k) clearance on 1981-05-11, under 510(k) number K803154.

Who is the listed applicant for INSTRUMENT CLEANER LIQUID CONCENTRATE?

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

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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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