FDA 510(k)

TAP 3, TAP 1

K 號：K160239 · 2016-08-10

決定日期2016-08-10

產品代碼PLC

諮詢委員會DE

決定相當於

器材摘要

TAP 3, TAP 1 is the device name listed in this FDA 510(k) record. The listed applicant is Airway Management, Inc.. It received FDA 510(k) clearance on 2016-08-10 under 510(k) number K160239. The device is classified under product code PLC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the TAP 3, TAP 1?

TAP 3, TAP 1 is a medical device that received FDA 510(k) clearance on 2016-08-10. The listed applicant is Airway Management, Inc.. The 510(k) number is K160239.

When did TAP 3, TAP 1 receive FDA 510(k) clearance?

TAP 3, TAP 1 received FDA 510(k) clearance on 2016-08-10, under 510(k) number K160239.

Who is the listed applicant for TAP 3, TAP 1?

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

What is the FDA product code for TAP 3, TAP 1?

The FDA product code for TAP 3, TAP 1 is PLC.

其他以 Airway Management, Inc. 為申請人之記錄

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K181482myTAP2

相關器械（代碼：PLC）

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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