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FDA 510(k)

LUER LOCKING ADAPTER(MATERIAL CHANGE)

K-Number: K840815 · 1984-11-08

ApplicantQuinton, Inc.
Decision Date1984-11-08
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LUER LOCKING ADAPTER(MATERIAL CHANGE) is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1984-11-08 under 510(k) number K840815. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUER LOCKING ADAPTER(MATERIAL CHANGE)?

LUER LOCKING ADAPTER(MATERIAL CHANGE) is a medical device that received FDA 510(k) clearance on 1984-11-08. The listed applicant is Quinton, Inc.. The 510(k) number is K840815.

When did LUER LOCKING ADAPTER(MATERIAL CHANGE) receive FDA 510(k) clearance?

LUER LOCKING ADAPTER(MATERIAL CHANGE) received FDA 510(k) clearance on 1984-11-08, under 510(k) number K840815.

Who is the listed applicant for LUER LOCKING ADAPTER(MATERIAL CHANGE)?

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

What is the FDA product code for LUER LOCKING ADAPTER(MATERIAL CHANGE)?

The FDA product code for LUER LOCKING ADAPTER(MATERIAL CHANGE) is FOZ.

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Other records listing Quinton, 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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