Medline Luer Lock Syringes
K-Number: K230235 · 2024-02-16
ApplicantMedline Industries, LP
Decision Date2024-02-16
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Medline Luer Lock Syringes is a medical device manufactured by Medline Industries, LP. It received FDA 510(k) clearance on 2024-02-16 under approval number K230235. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Medline Luer Lock Syringes?
Medline Luer Lock Syringes is a medical device that received FDA 510(k) clearance on 2024-02-16. It is manufactured by Medline Industries, LP. The 510(k) number is K230235.
When was Medline Luer Lock Syringes approved by the FDA?
Medline Luer Lock Syringes received FDA 510(k) clearance on 2024-02-16, under approval number K230235.
What company makes Medline Luer Lock Syringes?
Medline Luer Lock Syringes is manufactured by Medline Industries, LP.
What is the FDA product code for Medline Luer Lock Syringes?
The FDA product code for Medline Luer Lock Syringes is FMF.
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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.