FDA 510(k)

Neteera 130H-Plus 頻脈監測感測器

K 號：K231733 · 2024-02-09

決定日期2024-02-09

產品代碼DRT

諮詢委員會履歷

決定相當於

器材摘要

Neteera 130H-Plus Vital Sign Monitoring Sensor is the device name listed in this FDA 510(k) record. The listed applicant is Neteera Technologies , Ltd.. It received FDA 510(k) clearance on 2024-02-09 under 510(k) number K231733. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Neteera 130H-Plus Vital Sign Monitoring Sensor?

Neteera 130H-Plus Vital Sign Monitoring Sensor is a medical device that received FDA 510(k) clearance on 2024-02-09. The listed applicant is Neteera Technologies , Ltd.. The 510(k) number is K231733.

When did Neteera 130H-Plus Vital Sign Monitoring Sensor receive FDA 510(k) clearance?

Neteera 130H-Plus Vital Sign Monitoring Sensor received FDA 510(k) clearance on 2024-02-09, under 510(k) number K231733.

Who is the listed applicant for Neteera 130H-Plus Vital Sign Monitoring Sensor?

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

What is the FDA product code for Neteera 130H-Plus Vital Sign Monitoring Sensor?

The FDA product code for Neteera 130H-Plus Vital Sign Monitoring Sensor is DRT.

其他以 Neteera Technologies , Ltd. 為申請人之記錄

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K212143Neteera 130H/131H 頻脈監測感測器

相關器械（代碼：DRT）

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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