FDA 510(k)

Percutaneous Introducer Needle

Número K: K191295 · 2019-08-06

Data da decisão2019-08-06

Código do produtoGCJ

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Percutaneous Introducer Needle is the device name listed in this FDA 510(k) record. The listed applicant is Progressive Medical, Inc.. It received FDA 510(k) clearance on 2019-08-06 under 510(k) number K191295. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Percutaneous Introducer Needle?

Percutaneous Introducer Needle is a medical device that received FDA 510(k) clearance on 2019-08-06. The listed applicant is Progressive Medical, Inc.. The 510(k) number is K191295.

When did Percutaneous Introducer Needle receive FDA 510(k) clearance?

Percutaneous Introducer Needle received FDA 510(k) clearance on 2019-08-06, under 510(k) number K191295.

Who is the listed applicant for Percutaneous Introducer Needle?

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

What is the FDA product code for Percutaneous Introducer Needle?

The FDA product code for Percutaneous Introducer Needle is GCJ.

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