FDA 510(k)

PTFE超級鞘導管引導器 2.1

K 號：K153246 · 2016-02-12

決定日期2016-02-12

產品代碼DYB

諮詢委員會履歷

決定相當於

器材摘要

PTFE Super Sheath Introducer 2.1 is the device name listed in this FDA 510(k) record. The listed applicant is Medcomp (Medical Components, Inc.). It received FDA 510(k) clearance on 2016-02-12 under 510(k) number K153246. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the PTFE Super Sheath Introducer 2.1?

PTFE Super Sheath Introducer 2.1 is a medical device that received FDA 510(k) clearance on 2016-02-12. The listed applicant is Medcomp (Medical Components, Inc.). The 510(k) number is K153246.

When did PTFE Super Sheath Introducer 2.1 receive FDA 510(k) clearance?

PTFE Super Sheath Introducer 2.1 received FDA 510(k) clearance on 2016-02-12, under 510(k) number K153246.

Who is the listed applicant for PTFE Super Sheath Introducer 2.1?

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

What is the FDA product code for PTFE Super Sheath Introducer 2.1?

The FDA product code for PTFE Super Sheath Introducer 2.1 is DYB.

其他以 Medcomp (Medical Components, Inc.) 為申請人之記錄

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相關器械（代碼：DYB）

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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