FDA 510(k)

Vented Vial Adapter Transfer Device - 13mm

Número K: K160503 · 2016-05-04

RequerenteMedimop Medical Projects, Ltd.

Data da decisão2016-05-04

Código do produtoLHI

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Vented Vial Adapter Transfer Device - 13mm is the device name listed in this FDA 510(k) record. The listed applicant is Medimop Medical Projects, Ltd.. It received FDA 510(k) clearance on 2016-05-04 under 510(k) number K160503. The device is classified under product code LHI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Vented Vial Adapter Transfer Device - 13mm?

Vented Vial Adapter Transfer Device - 13mm is a medical device that received FDA 510(k) clearance on 2016-05-04. The listed applicant is Medimop Medical Projects, Ltd.. The 510(k) number is K160503.

When did Vented Vial Adapter Transfer Device - 13mm receive FDA 510(k) clearance?

Vented Vial Adapter Transfer Device - 13mm received FDA 510(k) clearance on 2016-05-04, under 510(k) number K160503.

Who is the listed applicant for Vented Vial Adapter Transfer Device - 13mm?

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

What is the FDA product code for Vented Vial Adapter Transfer Device - 13mm?

The FDA product code for Vented Vial Adapter Transfer Device - 13mm is LHI.

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Fonte oficial

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