FDA 510(k)

Aesculap Caiman 12 Tecnologia de Selamento e Corte

Número K: K203461 · 2020-12-18

Data da decisão2020-12-18

Código do produtoGEI

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Aesculap Caiman 12 Seal and Cut Technology System is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2020-12-18 under 510(k) number K203461. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Aesculap Caiman 12 Seal and Cut Technology System?

Aesculap Caiman 12 Seal and Cut Technology System is a medical device that received FDA 510(k) clearance on 2020-12-18. The listed applicant is Aesculap, Inc.. The 510(k) number is K203461.

When did Aesculap Caiman 12 Seal and Cut Technology System receive FDA 510(k) clearance?

Aesculap Caiman 12 Seal and Cut Technology System received FDA 510(k) clearance on 2020-12-18, under 510(k) number K203461.

Who is the listed applicant for Aesculap Caiman 12 Seal and Cut Technology System?

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

What is the FDA product code for Aesculap Caiman 12 Seal and Cut Technology System?

The FDA product code for Aesculap Caiman 12 Seal and Cut Technology System is GEI.

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Fonte oficial

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