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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, LP. It received FDA 510(k) clearance on 2024-02-16 under 510(k) 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. The listed applicant is Medline Industries, LP. The 510(k) number is K230235.

When did Medline Luer Lock Syringes receive FDA 510(k) clearance?

Medline Luer Lock Syringes received FDA 510(k) clearance on 2024-02-16, under 510(k) number K230235.

Who is the listed applicant for Medline Luer Lock Syringes?

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

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.

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