FDA 510(k)

1417WCC_127um 和 1417WCC_140um

K 號：K171418 · 2017-06-12

決定日期2017-06-12

產品代碼MQB

諮詢委員會RA

決定相當於

器材摘要

1417WCC_127um and1417WCC_140um is the device name listed in this FDA 510(k) record. The listed applicant is Rayence Co., Ltd.. It received FDA 510(k) clearance on 2017-06-12 under 510(k) number K171418. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the 1417WCC_127um and1417WCC_140um?

1417WCC_127um and1417WCC_140um is a medical device that received FDA 510(k) clearance on 2017-06-12. The listed applicant is Rayence Co., Ltd.. The 510(k) number is K171418.

When did 1417WCC_127um and1417WCC_140um receive FDA 510(k) clearance?

1417WCC_127um and1417WCC_140um received FDA 510(k) clearance on 2017-06-12, under 510(k) number K171418.

Who is the listed applicant for 1417WCC_127um and1417WCC_140um?

FDA 510(k) 記錄將 Rayence Co., Ltd. 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for 1417WCC_127um and1417WCC_140um?

The FDA product code for 1417WCC_127um and1417WCC_140um is MQB.