FDA 510(k)

Carilex VT¿200-i NX

K 號：K231646 · 2024-04-17

決定日期2024-04-17

產品代碼OMP

諮詢委員會SU 請提供完整的描述文本，以便我進行翻譯。

決定相當於

器材摘要

Carilex VT¿200-i NX is the device name listed in this FDA 510(k) record. The listed applicant is Carilex Medical, Inc.. It received FDA 510(k) clearance on 2024-04-17 under 510(k) number K231646. The device is classified under product code OMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Carilex VT¿200-i NX?

Carilex VT¿200-i NX is a medical device that received FDA 510(k) clearance on 2024-04-17. The listed applicant is Carilex Medical, Inc.. The 510(k) number is K231646.

When did Carilex VT¿200-i NX receive FDA 510(k) clearance?

Carilex VT¿200-i NX received FDA 510(k) clearance on 2024-04-17, under 510(k) number K231646.

Who is the listed applicant for Carilex VT¿200-i NX?

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

What is the FDA product code for Carilex VT¿200-i NX?

The FDA product code for Carilex VT¿200-i NX is OMP.

其他以 Carilex Medical, Inc. 為申請人之記錄

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

K173407VT - 100, VT - 200 K172725VT 製藥包 K161410VT·One, VT·One 60天

相關器械（代碼：OMP）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

K261338RENASYS DYNAFLOW 套件（66807741）Smith & Nephew Medical, Ltd.K253263ConvaVAC™ 負壓傷口治療系統Convatec Limited, Gdc Building K253199CURASYS 2 (EMDN0003)CG Bio Co., Ltd.K260646RENASYS EDGE (66803126)Smith & Nephew Medical, Ltd.K261291Nisus NPWT 內容器 500-mL (CPC-500)Cork Medical K254019傷口基因NPWT系統Bechtel Medical, Inc.

官方來源

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。