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FDA 510(k)

Female Luer Lock Cap

K-Number: K200425 · 2020-10-29

ApplicantMedsafety Solutions, LLC
Decision Date2020-10-29
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Female Luer Lock Cap is the device name listed in this FDA 510(k) record. The listed applicant is Medsafety Solutions, LLC. It received FDA 510(k) clearance on 2020-10-29 under 510(k) number K200425. 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 Female Luer Lock Cap?

Female Luer Lock Cap is a medical device that received FDA 510(k) clearance on 2020-10-29. The listed applicant is Medsafety Solutions, LLC. The 510(k) number is K200425.

When did Female Luer Lock Cap receive FDA 510(k) clearance?

Female Luer Lock Cap received FDA 510(k) clearance on 2020-10-29, under 510(k) number K200425.

Who is the listed applicant for Female Luer Lock Cap?

The FDA 510(k) record lists Medsafety Solutions, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Female Luer Lock Cap?

The FDA product code for Female Luer Lock Cap is FPA.

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.

K261530iiSure Infusion SetDeka Research and DevelopmentK252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)Amsino International, Inc.K251375PuraCath Firefly Needleless Connector IT (9005)Puracath Medical, Inc.K251257nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free Connector (NFC) [6426731]; nSyte Needle Free Connector (NFC) [6426727]Np MedicalK250325BD Alaris Pump Infusion SetCarefusion (Bd)K251814EZ™ IV Administration SetEpic Medical Pte. , Ltd.

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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