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FDA 510(k)

CapsoCam Plus (SV-3) Capsule Endoscopy System

K 號:K192662 · 2020-02-14

決定日期2020-02-14
產品代碼NEZ
諮詢委員會GU
決定Substantially Equivalent

器材摘要

CapsoCam Plus (SV-3) Capsule Endoscopy System is the device name listed in this FDA 510(k) record. The listed applicant is CapsoVision, Inc.. It received FDA 510(k) clearance on 2020-02-14 under 510(k) number K192662. The device is classified under product code NEZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the CapsoCam Plus (SV-3) Capsule Endoscopy System?

CapsoCam Plus (SV-3) Capsule Endoscopy System is a medical device that received FDA 510(k) clearance on 2020-02-14. The listed applicant is CapsoVision, Inc.. The 510(k) number is K192662.

When did CapsoCam Plus (SV-3) Capsule Endoscopy System receive FDA 510(k) clearance?

CapsoCam Plus (SV-3) Capsule Endoscopy System received FDA 510(k) clearance on 2020-02-14, under 510(k) number K192662.

Who is the listed applicant for CapsoCam Plus (SV-3) Capsule Endoscopy System?

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

What is the FDA product code for CapsoCam Plus (SV-3) Capsule Endoscopy System?

The FDA product code for CapsoCam Plus (SV-3) Capsule Endoscopy System is NEZ.

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其他以 CapsoVision, Inc. 為申請人之記錄

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相關器械(代碼:NEZ)

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官方來源

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