Q-FLO CLOSED MALE LUER CONNECTOR
K-Number: K121554 · 2012-06-08
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Device Summary
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
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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