FDA 510(k)

basixTOUCH40 Inflation Syringe

Número K: K153672 · 2016-01-20

Data da decisão2016-01-20

Código do produtoMAV

Comité consultivoCV

DecisãoUnknown

Resumo do dispositivo

basixTOUCH40 Inflation Syringe is the device name listed in this FDA 510(k) record. The listed applicant is Merit Medical Systems, Inc.. It received FDA 510(k) clearance on 2016-01-20 under 510(k) number K153672. The device is classified under product code MAV. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Perguntas frequentes

What is the basixTOUCH40 Inflation Syringe?

basixTOUCH40 Inflation Syringe is a medical device that received FDA 510(k) clearance on 2016-01-20. The listed applicant is Merit Medical Systems, Inc.. The 510(k) number is K153672.

When did basixTOUCH40 Inflation Syringe receive FDA 510(k) clearance?

basixTOUCH40 Inflation Syringe received FDA 510(k) clearance on 2016-01-20, under 510(k) number K153672.

Who is the listed applicant for basixTOUCH40 Inflation Syringe?

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

What is the FDA product code for basixTOUCH40 Inflation Syringe?

The FDA product code for basixTOUCH40 Inflation Syringe is MAV.

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Fonte oficial

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