FDA 510(k)

最小侵襲的前立腺手術ナビゲーションシステム（モデル：AmaKris SR1-A-2）

K番号: K242314 · 2025-09-11

申請者Augment Intelligent Medical System (China) Co., Ltd.

決定日2025-09-11

製品コードLLZ

諮問委員会RA （注：由于原文中未提供具体的医疗设备监管文本内容，因此无法进行翻译。请提供具体的文本内容以便进行翻译。）

決定大幅同等

医療機器の概要

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.

よくある質問

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.

申請者としてAugment Intelligent Medical System (China) Co., Ltd.を記載するその他の記録

K221499最小侵襲的前立腺手術ナビゲーションシステム

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