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FDA 510(k)

3 PORT LUER

K-Number: K770500 · 1977-04-05

ApplicantUnimetrics Corp.
Decision Date1977-04-05
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

3 PORT LUER is the device name listed in this FDA 510(k) record. The listed applicant is Unimetrics Corp.. It received FDA 510(k) clearance on 1977-04-05 under 510(k) number K770500. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3 PORT LUER?

3 PORT LUER is a medical device that received FDA 510(k) clearance on 1977-04-05. The listed applicant is Unimetrics Corp.. The 510(k) number is K770500.

When did 3 PORT LUER receive FDA 510(k) clearance?

3 PORT LUER received FDA 510(k) clearance on 1977-04-05, under 510(k) number K770500.

Who is the listed applicant for 3 PORT LUER?

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

What is the FDA product code for 3 PORT LUER?

The FDA product code for 3 PORT LUER is EOQ.

Other records listing Unimetrics Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K760500TUBE, HEAVY GLASS WALL INJECTION

Related Devices (Code: EOQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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