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FDA 510(k)

Q-FLO CLOSED MALE LUER CONNECTOR

K-Number: K121554 · 2012-06-08

Decision Date2012-06-08
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Q-FLO CLOSED MALE LUER CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Us Fusion, LLC. Dba Truecare Biomedix-USA. It received FDA 510(k) clearance on 2012-06-08 under 510(k) number K121554. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Q-FLO CLOSED MALE LUER CONNECTOR?

Q-FLO CLOSED MALE LUER CONNECTOR is a medical device that received FDA 510(k) clearance on 2012-06-08. The listed applicant is Us Fusion, LLC. Dba Truecare Biomedix-USA. The 510(k) number is K121554.

When did Q-FLO CLOSED MALE LUER CONNECTOR receive FDA 510(k) clearance?

Q-FLO CLOSED MALE LUER CONNECTOR received FDA 510(k) clearance on 2012-06-08, under 510(k) number K121554.

Who is the listed applicant for Q-FLO CLOSED MALE LUER CONNECTOR?

The FDA 510(k) record lists Us Fusion, LLC. Dba Truecare Biomedix-USA as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Q-FLO CLOSED MALE LUER CONNECTOR?

The FDA product code for Q-FLO CLOSED MALE LUER CONNECTOR is FPA.

Related Clinical Trials

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.

Related Devices (Code: FPA)

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.

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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