FDA 510(k)

UltraCath Continuous Nerve block Catheter

Número K: K162522 · 2017-03-17

Data da decisão2017-03-17

Código do produtoBSO

Comité consultivoAN

DecisãoSubstantially Equivalent

Resumo do dispositivo

UltraCath Continuous Nerve block Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Teleflexmedical, Inc.. It received FDA 510(k) clearance on 2017-03-17 under 510(k) number K162522. The device is classified under product code BSO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the UltraCath Continuous Nerve block Catheter?

UltraCath Continuous Nerve block Catheter is a medical device that received FDA 510(k) clearance on 2017-03-17. The listed applicant is Teleflexmedical, Inc.. The 510(k) number is K162522.

When did UltraCath Continuous Nerve block Catheter receive FDA 510(k) clearance?

UltraCath Continuous Nerve block Catheter received FDA 510(k) clearance on 2017-03-17, under 510(k) number K162522.

Who is the listed applicant for UltraCath Continuous Nerve block Catheter?

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

What is the FDA product code for UltraCath Continuous Nerve block Catheter?

The FDA product code for UltraCath Continuous Nerve block Catheter is BSO.

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Fonte oficial

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