FDA 510(k)

Minimally Invasive Prostate Surgery Navigation System(Model:AmaKris SR1-A-2)

Número K: K242314 · 2025-09-11

RequerenteAugment Intelligent Medical System (China) Co., Ltd.

Data da decisão2025-09-11

Código do produtoLLZ

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do dispositivo

Minimally Invasive Prostate Surgery Navigation System(Model:AmaKris SR1-A-2) is the device name listed in this FDA 510(k) record. The listed applicant is Augment Intelligent Medical System (China) Co., Ltd.. It received FDA 510(k) clearance on 2025-09-11 under 510(k) number K242314. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Minimally Invasive Prostate Surgery Navigation System(Model:AmaKris SR1-A-2)?

Minimally Invasive Prostate Surgery Navigation System(Model:AmaKris SR1-A-2) is a medical device that received FDA 510(k) clearance on 2025-09-11. The listed applicant is Augment Intelligent Medical System (China) Co., Ltd.. The 510(k) number is K242314.

When did Minimally Invasive Prostate Surgery Navigation System(Model:AmaKris SR1-A-2) receive FDA 510(k) clearance?

Minimally Invasive Prostate Surgery Navigation System(Model:AmaKris SR1-A-2) received FDA 510(k) clearance on 2025-09-11, under 510(k) number K242314.

Who is the listed applicant for Minimally Invasive Prostate Surgery Navigation System(Model:AmaKris SR1-A-2)?

The FDA 510(k) record lists Augment Intelligent Medical System (China) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Minimally Invasive Prostate Surgery Navigation System(Model:AmaKris SR1-A-2)?

The FDA product code for Minimally Invasive Prostate Surgery Navigation System(Model:AmaKris SR1-A-2) is LLZ.

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Outros registros que listam Augment Intelligent Medical System (China) Co., Ltd. como candidato(a)

K221499Minimally Invasive Prostate Surgery Navigation System

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Fonte oficial

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