FDA 510(k)

KARL STORZ NAV1 Electromagnetic Navigation System

Número K: K161555 · 2016-10-21

RequerenteKarl Storz Endoscopy America, Inc.

Data da decisão2016-10-21

Código do produtoPGW

Comité consultivoNE

DecisãoSubstantially Equivalent

Resumo do dispositivo

KARL STORZ NAV1 Electromagnetic Navigation System is the device name listed in this FDA 510(k) record. The listed applicant is Karl Storz Endoscopy America, Inc.. It received FDA 510(k) clearance on 2016-10-21 under 510(k) number K161555. The device is classified under product code PGW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the KARL STORZ NAV1 Electromagnetic Navigation System?

KARL STORZ NAV1 Electromagnetic Navigation System is a medical device that received FDA 510(k) clearance on 2016-10-21. The listed applicant is Karl Storz Endoscopy America, Inc.. The 510(k) number is K161555.

When did KARL STORZ NAV1 Electromagnetic Navigation System receive FDA 510(k) clearance?

KARL STORZ NAV1 Electromagnetic Navigation System received FDA 510(k) clearance on 2016-10-21, under 510(k) number K161555.

Who is the listed applicant for KARL STORZ NAV1 Electromagnetic Navigation System?

The FDA 510(k) record lists Karl Storz Endoscopy America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KARL STORZ NAV1 Electromagnetic Navigation System?

The FDA product code for KARL STORZ NAV1 Electromagnetic Navigation System is PGW.

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Fonte oficial

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