FDA 510(k)

Tec 820, Tec 850

K 號：K172702 · 2018-01-04

決定日期2018-01-04

產品代碼CAD

諮詢委員會AN

決定相當於

器材摘要

Tec 820, Tec 850 is the device name listed in this FDA 510(k) record. The listed applicant is Datex-Ohmeda, Inc.. It received FDA 510(k) clearance on 2018-01-04 under 510(k) number K172702. The device is classified under product code CAD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Tec 820, Tec 850?

Tec 820, Tec 850 is a medical device that received FDA 510(k) clearance on 2018-01-04. The listed applicant is Datex-Ohmeda, Inc.. The 510(k) number is K172702.

When did Tec 820, Tec 850 receive FDA 510(k) clearance?

Tec 820, Tec 850 received FDA 510(k) clearance on 2018-01-04, under 510(k) number K172702.

Who is the listed applicant for Tec 820, Tec 850?

FDA 510(k) 記錄將 Datex-Ohmeda, Inc. 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Tec 820, Tec 850?

The FDA product code for Tec 820, Tec 850 is CAD.