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FDA 510(k)

Arrow Seldinger Arterial Catheterization Device 18 ga., Arrow Seldinger Arterial Catheterization Device 20 ga., Arrow Seldinger Arterial Catheterization Device 22 ga., Arrow Seldinger Arterial Catheterization Device 24 ga.

Número K: K171146 · 2017-06-23

RequerenteArrow International, Inc. (Subsidiary of Telelflex Inc.)
Data da decisão2017-06-23
Código do produtoDQY
Comité consultivoCV
DecisãoSubstantially Equivalent

Resumo do dispositivo

Arrow Seldinger Arterial Catheterization Device 18 ga., Arrow Seldinger Arterial Catheterization Device 20 ga., Arrow Seldinger Arterial Catheterization Device 22 ga., Arrow Seldinger Arterial Catheterization Device 24 ga. is the device name listed in this FDA 510(k) record. The listed applicant is Arrow International, Inc. (Subsidiary of Telelflex Inc.). It received FDA 510(k) clearance on 2017-06-23 under 510(k) number K171146. 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 Arrow Seldinger Arterial Catheterization Device 18 ga., Arrow Seldinger Arterial Catheterization Device 20 ga., Arrow Seldinger Arterial Catheterization Device 22 ga., Arrow Seldinger Arterial Catheterization Device 24 ga.?

Arrow Seldinger Arterial Catheterization Device 18 ga., Arrow Seldinger Arterial Catheterization Device 20 ga., Arrow Seldinger Arterial Catheterization Device 22 ga., Arrow Seldinger Arterial Catheterization Device 24 ga. is a medical device that received FDA 510(k) clearance on 2017-06-23. The listed applicant is Arrow International, Inc. (Subsidiary of Telelflex Inc.). The 510(k) number is K171146.

When did Arrow Seldinger Arterial Catheterization Device 18 ga., Arrow Seldinger Arterial Catheterization Device 20 ga., Arrow Seldinger Arterial Catheterization Device 22 ga., Arrow Seldinger Arterial Catheterization Device 24 ga. receive FDA 510(k) clearance?

Arrow Seldinger Arterial Catheterization Device 18 ga., Arrow Seldinger Arterial Catheterization Device 20 ga., Arrow Seldinger Arterial Catheterization Device 22 ga., Arrow Seldinger Arterial Catheterization Device 24 ga. received FDA 510(k) clearance on 2017-06-23, under 510(k) number K171146.

Who is the listed applicant for Arrow Seldinger Arterial Catheterization Device 18 ga., Arrow Seldinger Arterial Catheterization Device 20 ga., Arrow Seldinger Arterial Catheterization Device 22 ga., Arrow Seldinger Arterial Catheterization Device 24 ga.?

The FDA 510(k) record lists Arrow International, Inc. (Subsidiary of Telelflex Inc.) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Arrow Seldinger Arterial Catheterization Device 18 ga., Arrow Seldinger Arterial Catheterization Device 20 ga., Arrow Seldinger Arterial Catheterization Device 22 ga., Arrow Seldinger Arterial Catheterization Device 24 ga.?

The FDA product code for Arrow Seldinger Arterial Catheterization Device 18 ga., Arrow Seldinger Arterial Catheterization Device 20 ga., Arrow Seldinger Arterial Catheterization Device 22 ga., Arrow Seldinger Arterial Catheterization Device 24 ga. is DQY.

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Dispositivos Relacionados (Código: DQY)

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Fonte oficial

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