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FDA 510(k)

Turnpike Catheter; Turnpike Spiral Catheter; Turnpike Gold Catheter; Turnpike LP Catheter

Número K: K191560 · 2019-08-09

RequerenteVascular Solutions, LLC
Data da decisão2019-08-09
Código do produtoDQY
Comité consultivoCV
DecisãoSubstantially Equivalent

Resumo do dispositivo

Turnpike Catheter; Turnpike Spiral Catheter; Turnpike Gold Catheter; Turnpike LP Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Solutions, LLC. It received FDA 510(k) clearance on 2019-08-09 under 510(k) number K191560. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Turnpike Catheter; Turnpike Spiral Catheter; Turnpike Gold Catheter; Turnpike LP Catheter?

Turnpike Catheter; Turnpike Spiral Catheter; Turnpike Gold Catheter; Turnpike LP Catheter is a medical device that received FDA 510(k) clearance on 2019-08-09. The listed applicant is Vascular Solutions, LLC. The 510(k) number is K191560.

When did Turnpike Catheter; Turnpike Spiral Catheter; Turnpike Gold Catheter; Turnpike LP Catheter receive FDA 510(k) clearance?

Turnpike Catheter; Turnpike Spiral Catheter; Turnpike Gold Catheter; Turnpike LP Catheter received FDA 510(k) clearance on 2019-08-09, under 510(k) number K191560.

Who is the listed applicant for Turnpike Catheter; Turnpike Spiral Catheter; Turnpike Gold Catheter; Turnpike LP Catheter?

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

What is the FDA product code for Turnpike Catheter; Turnpike Spiral Catheter; Turnpike Gold Catheter; Turnpike LP Catheter?

The FDA product code for Turnpike Catheter; Turnpike Spiral Catheter; Turnpike Gold Catheter; Turnpike LP Catheter is DQY.

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Outros registros que listam Vascular Solutions, LLC como candidato(a)

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Dispositivos Relacionados (Código: DQY)

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Fonte oficial

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