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FDA 510(k)

INSTRUMENT LUBRICANT

K-Number: K780610 · 1978-05-31

ApplicantAbco Dealers, Inc.
Decision Date1978-05-31
Product Code
DecisionSubstantially Equivalent

Device Summary

INSTRUMENT LUBRICANT 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 1978-05-31 under 510(k) number K780610. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTRUMENT LUBRICANT?

INSTRUMENT LUBRICANT is a medical device that received FDA 510(k) clearance on 1978-05-31. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K780610.

When did INSTRUMENT LUBRICANT receive FDA 510(k) clearance?

INSTRUMENT LUBRICANT received FDA 510(k) clearance on 1978-05-31, under 510(k) number K780610.

Who is the listed applicant for INSTRUMENT LUBRICANT?

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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