FDA 510(k)

Ranfac Cartilage Biopsy Needle

Número K: K183146 · 2019-04-25

Data da decisão2019-04-25

Código do produtoKNW

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Ranfac Cartilage Biopsy Needle is the device name listed in this FDA 510(k) record. The listed applicant is Ranfac Corporation. It received FDA 510(k) clearance on 2019-04-25 under 510(k) number K183146. 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 Cartilage Biopsy Needle?

Ranfac Cartilage Biopsy Needle is a medical device that received FDA 510(k) clearance on 2019-04-25. The listed applicant is Ranfac Corporation. The 510(k) number is K183146.

When did Ranfac Cartilage Biopsy Needle receive FDA 510(k) clearance?

Ranfac Cartilage Biopsy Needle received FDA 510(k) clearance on 2019-04-25, under 510(k) number K183146.

Who is the listed applicant for Ranfac Cartilage Biopsy Needle?

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 Cartilage Biopsy Needle?

The FDA product code for Ranfac Cartilage Biopsy Needle is KNW.

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Outros registros que listam Ranfac Corporation como candidato(a)

K223612Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA)K202287Ran-Flex-B Bone Marrow Aspiration Needle K190177J-Type Marrow Biopsy Needle,T-Type Marrow Biopsy Needle,Tweezer Bone Marrow Biopsy Needle,

Dispositivos Relacionados (Código: KNW)

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