FDA 510(k)

ProSeal™ Injection Site Extended Male Luer Lock (422140)

K-번호: K240433 · 2024-05-21

결정일2024-05-21

제품 코드ONB

자문 위원회HO

결정Substantially Equivalent

기기 요약

ProSeal™ Injection Site Extended Male Luer Lock (422140) is the device name listed in this FDA 510(k) record. The listed applicant is Epic Medical Pte. , Ltd.. It received FDA 510(k) clearance on 2024-05-21 under 510(k) number K240433. The device is classified under product code ONB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the ProSeal™ Injection Site Extended Male Luer Lock (422140)?

ProSeal™ Injection Site Extended Male Luer Lock (422140) is a medical device that received FDA 510(k) clearance on 2024-05-21. The listed applicant is Epic Medical Pte. , Ltd.. The 510(k) number is K240433.

When did ProSeal™ Injection Site Extended Male Luer Lock (422140) receive FDA 510(k) clearance?

ProSeal™ Injection Site Extended Male Luer Lock (422140) received FDA 510(k) clearance on 2024-05-21, under 510(k) number K240433.

Who is the listed applicant for ProSeal™ Injection Site Extended Male Luer Lock (422140)?

The FDA 510(k) record lists Epic Medical Pte. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ProSeal™ Injection Site Extended Male Luer Lock (422140)?

The FDA product code for ProSeal™ Injection Site Extended Male Luer Lock (422140) is ONB.

Epic Medical Pte. , Ltd.를 신청인으로 등재한 기타 기록

K252987ADRx® Admixture Device K250234SMARTeZ™ Elastomeric Infusion Pump (RS series)K251722ProSeal™ Transfer Injector (421120, 421130, 421140)K251814EZ™ IV Administration Set K252094eZSURE™ Empty Fluid Container K251340ProSeal™ Bag Spike with Additive Port (423370ST, 423370)

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