FDA 510(k)

cCeLL - 適用於體內

K 號：K233391 · 2024-08-21

決定日期2024-08-21

產品代碼GWG

諮詢委員會NE (請提供完整的英文描述，以便進行翻譯。)

決定相當於

器材摘要

cCeLL - In vivo is the device name listed in this FDA 510(k) record. The listed applicant is VPIX Medical, Inc.. It received FDA 510(k) clearance on 2024-08-21 under 510(k) number K233391. The device is classified under product code GWG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the cCeLL - In vivo?

cCeLL - In vivo is a medical device that received FDA 510(k) clearance on 2024-08-21. The listed applicant is VPIX Medical, Inc.. The 510(k) number is K233391.

When did cCeLL - In vivo receive FDA 510(k) clearance?

cCeLL - In vivo received FDA 510(k) clearance on 2024-08-21, under 510(k) number K233391.

Who is the listed applicant for cCeLL - In vivo?

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

What is the FDA product code for cCeLL - In vivo?

The FDA product code for cCeLL - In vivo is GWG.

其他以 VPIX Medical, Inc. 為申請人之記錄

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K251852cCeLL - 適用於In vivo與Drop-In Robo (CN100-2W2C488775, CN100-1W1C775, DR200)

相關器械（代碼：GWG）

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官方來源

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