FDA 510(k)

The POD

K 號：K182820 · 2019-07-17

決定日期2019-07-17

產品代碼MQC

決定相當於

器材摘要

The POD is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Facialdontics, LLC. It received FDA 510(k) clearance on 2019-07-17 under 510(k) number K182820. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.

常見問題

What is the The POD?

The POD is a medical device that received FDA 510(k) clearance on 2019-07-17. The listed applicant is Advanced Facialdontics, LLC. The 510(k) number is K182820.

When did The POD receive FDA 510(k) clearance?

The POD received FDA 510(k) clearance on 2019-07-17, under 510(k) number K182820.

Who is the listed applicant for The POD?

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

What is the FDA product code for The POD?

The FDA product code for The POD is MQC.

其他以 Advanced Facialdontics, LLC 為申請人之記錄

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相關器械（代碼：MQC）

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