FDA 510(k)

CDB 自鍊結合器 8F

K 號：K160957 · 2016-09-27

決定日期2016-09-27

產品代碼NJM

諮詢委員會DE

決定相當於

器材摘要

CDB Self Ligating Bracket 8F is the device name listed in this FDA 510(k) record. The listed applicant is Cdb Corporation. It received FDA 510(k) clearance on 2016-09-27 under 510(k) number K160957. The device is classified under product code NJM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the CDB Self Ligating Bracket 8F?

CDB Self Ligating Bracket 8F is a medical device that received FDA 510(k) clearance on 2016-09-27. The listed applicant is Cdb Corporation. The 510(k) number is K160957.

When did CDB Self Ligating Bracket 8F receive FDA 510(k) clearance?

CDB Self Ligating Bracket 8F received FDA 510(k) clearance on 2016-09-27, under 510(k) number K160957.

Who is the listed applicant for CDB Self Ligating Bracket 8F?

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

What is the FDA product code for CDB Self Ligating Bracket 8F?

The FDA product code for CDB Self Ligating Bracket 8F is NJM.

其他以 Cdb Corporation 為申請人之記錄

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