FDA 510(k)

前瞻精英模組組織脈搏血氧儀

K 號：K180003 · 2018-05-10

決定日期2018-05-10

產品代碼MUD

諮詢委員會履歷

決定相當於

器材摘要

FORE-SIGHT ELITE Module Tissue Oximeter is the device name listed in this FDA 510(k) record. The listed applicant is Cas Medical Systems, Inc.. It received FDA 510(k) clearance on 2018-05-10 under 510(k) number K180003. The device is classified under product code MUD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the FORE-SIGHT ELITE Module Tissue Oximeter?

FORE-SIGHT ELITE Module Tissue Oximeter is a medical device that received FDA 510(k) clearance on 2018-05-10. The listed applicant is Cas Medical Systems, Inc.. The 510(k) number is K180003.

When did FORE-SIGHT ELITE Module Tissue Oximeter receive FDA 510(k) clearance?

FORE-SIGHT ELITE Module Tissue Oximeter received FDA 510(k) clearance on 2018-05-10, under 510(k) number K180003.

Who is the listed applicant for FORE-SIGHT ELITE Module Tissue Oximeter?

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

What is the FDA product code for FORE-SIGHT ELITE Module Tissue Oximeter?

The FDA product code for FORE-SIGHT ELITE Module Tissue Oximeter is MUD.

其他以 Cas Medical Systems, 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。

K190270前瞻精英組織氧濃度測量模組

相關器械（代碼：MUD）

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。

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官方來源

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