FDA 510(k)

SteriCap Safety Needle; VitreJect Safety Needle

Número K: K233343 · 2023-11-27

Data da decisão2023-11-27

Código do produtoFMI

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

SteriCap Safety Needle; VitreJect Safety Needle is the device name listed in this FDA 510(k) record. The listed applicant is Ocuject, LLC. It received FDA 510(k) clearance on 2023-11-27 under 510(k) number K233343. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the SteriCap Safety Needle; VitreJect Safety Needle?

SteriCap Safety Needle; VitreJect Safety Needle is a medical device that received FDA 510(k) clearance on 2023-11-27. The listed applicant is Ocuject, LLC. The 510(k) number is K233343.

When did SteriCap Safety Needle; VitreJect Safety Needle receive FDA 510(k) clearance?

SteriCap Safety Needle; VitreJect Safety Needle received FDA 510(k) clearance on 2023-11-27, under 510(k) number K233343.

Who is the listed applicant for SteriCap Safety Needle; VitreJect Safety Needle?

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

What is the FDA product code for SteriCap Safety Needle; VitreJect Safety Needle?

The FDA product code for SteriCap Safety Needle; VitreJect Safety Needle is FMI.

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Outros registros que listam Ocuject, LLC como candidato(a)

K242956LDS Needle; OcuSafe® LDS Needle; SteriCap® LDS Safety Needle; VitreJect® LDS Safety Needle K230959VitreJect® Needle; OcuSafe® Needle K230372VitreJect Syringe K212544MiniLoad Syringe K212805SteriCap Mini Needle and Standard Needles K202432MiniLoad Syringe

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Dispositivos Relacionados (Código: FMI)

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Fonte oficial

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