FDA 510(k)

Vesco Medical NRFit Tip Syringes

Número K: K170218 · 2017-02-24

Data da decisão2017-02-24

Código do produtoFMF

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Vesco Medical NRFit Tip Syringes is the device name listed in this FDA 510(k) record. The listed applicant is Vesco Medical, LLC. It received FDA 510(k) clearance on 2017-02-24 under 510(k) number K170218. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Vesco Medical NRFit Tip Syringes?

Vesco Medical NRFit Tip Syringes is a medical device that received FDA 510(k) clearance on 2017-02-24. The listed applicant is Vesco Medical, LLC. The 510(k) number is K170218.

When did Vesco Medical NRFit Tip Syringes receive FDA 510(k) clearance?

Vesco Medical NRFit Tip Syringes received FDA 510(k) clearance on 2017-02-24, under 510(k) number K170218.

Who is the listed applicant for Vesco Medical NRFit Tip Syringes?

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

What is the FDA product code for Vesco Medical NRFit Tip Syringes?

The FDA product code for Vesco Medical NRFit Tip Syringes is FMF.

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Outros registros que listam Vesco Medical, LLC como candidato(a)

K232205Vesco Q™ Enteral Feeding Pump; Vesco Q™ 500mL Bag Feed Set; Vesco Q™ 1000mL Bag Feed Set; Vesco Q™ 40mm Screw Cap Feed Set; Vesco Q™ ENPlus Feed Set K192991Vesco Medical Extension Feeding Set K170162Vesco Medical Nasoenteric Feeding Tubes

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Fonte oficial

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