FDA 510(k)

Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA)

Número K: K223612 · 2023-02-21

Data da decisão2023-02-21

Código do produtoKNW

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA) is the device name listed in this FDA 510(k) record. The listed applicant is Ranfac Corporation. It received FDA 510(k) clearance on 2023-02-21 under 510(k) number K223612. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA)?

Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA) is a medical device that received FDA 510(k) clearance on 2023-02-21. The listed applicant is Ranfac Corporation. The 510(k) number is K223612.

When did Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA) receive FDA 510(k) clearance?

Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA) received FDA 510(k) clearance on 2023-02-21, under 510(k) number K223612.

Who is the listed applicant for Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA)?

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

What is the FDA product code for Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA)?

The FDA product code for Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA) is KNW.

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Outros registros que listam Ranfac Corporation como candidato(a)

K202287Ran-Flex-B Bone Marrow Aspiration Needle K190177J-Type Marrow Biopsy Needle,T-Type Marrow Biopsy Needle,Tweezer Bone Marrow Biopsy Needle,K183146Ranfac Cartilage Biopsy Needle

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