FDA 510(k)

091 長針，70 cm，091 長針，80 cm，091 長針，90 cm

K 號：K172468 · 2017-12-06

決定日期2017-12-06

產品代碼DQY

諮詢委員會履歷

決定相當於

器材摘要

091 Long Sheath, 70 cm, 091 Long Sheath, 80 cm, 091 Long Sheath, 90 cm is the device name listed in this FDA 510(k) record. The listed applicant is Inneuroco, Inc.. It received FDA 510(k) clearance on 2017-12-06 under 510(k) number K172468. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the 091 Long Sheath, 70 cm, 091 Long Sheath, 80 cm, 091 Long Sheath, 90 cm?

091 Long Sheath, 70 cm, 091 Long Sheath, 80 cm, 091 Long Sheath, 90 cm is a medical device that received FDA 510(k) clearance on 2017-12-06. The listed applicant is Inneuroco, Inc.. The 510(k) number is K172468.

When did 091 Long Sheath, 70 cm, 091 Long Sheath, 80 cm, 091 Long Sheath, 90 cm receive FDA 510(k) clearance?

091 Long Sheath, 70 cm, 091 Long Sheath, 80 cm, 091 Long Sheath, 90 cm received FDA 510(k) clearance on 2017-12-06, under 510(k) number K172468.

Who is the listed applicant for 091 Long Sheath, 70 cm, 091 Long Sheath, 80 cm, 091 Long Sheath, 90 cm?

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

What is the FDA product code for 091 Long Sheath, 70 cm, 091 Long Sheath, 80 cm, 091 Long Sheath, 90 cm?

The FDA product code for 091 Long Sheath, 70 cm, 091 Long Sheath, 80 cm, 091 Long Sheath, 90 cm is DQY.

其他以 Inneuroco, Inc. 為申請人之記錄

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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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