FDA 510(k)

ビデオ内視鏡システム、3Dビデオ内視鏡システム

K番号: K210116 · 2021-10-13

申請者Surgnova Healthcare Technologies (Zhejiang) Co., Ltd.

決定日2021-10-13

製品コードHET

諮問委員会医薬品機器規制テキストの翻訳は以下の通りです。 [原文] OB [翻訳] OB

決定大幅同等

医療機器の概要

Video Endoscopy System, 3D Video Endoscopy System is the device name listed in this FDA 510(k) record. The listed applicant is Surgnova Healthcare Technologies (Zhejiang) Co., Ltd.. It received FDA 510(k) clearance on 2021-10-13 under 510(k) number K210116. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Video Endoscopy System, 3D Video Endoscopy System?

Video Endoscopy System, 3D Video Endoscopy System is a medical device that received FDA 510(k) clearance on 2021-10-13. The listed applicant is Surgnova Healthcare Technologies (Zhejiang) Co., Ltd.. The 510(k) number is K210116.

When did Video Endoscopy System, 3D Video Endoscopy System receive FDA 510(k) clearance?

Video Endoscopy System, 3D Video Endoscopy System received FDA 510(k) clearance on 2021-10-13, under 510(k) number K210116.

Who is the listed applicant for Video Endoscopy System, 3D Video Endoscopy System?

The FDA 510(k) record lists Surgnova Healthcare Technologies (Zhejiang) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Video Endoscopy System, 3D Video Endoscopy System?

The FDA product code for Video Endoscopy System, 3D Video Endoscopy System is HET.

申請者としてSurgnova Healthcare Technologies (Zhejiang) Co., Ltd.を記載するその他の記録

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公式ソース

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