FDA 510(k)

ベネライフプレミアムフェイシャルケアパック、モデル：QZ0701A

K番号: K171647 · 2017-10-23

決定日2017-10-23

製品コードNFO

諮問委員会Please provide the source text to translate.

決定大幅同等

医療機器の概要

BeneLife Premium Facial Treatment Pack, Model: QZ0701A is the device name listed in this FDA 510(k) record. The listed applicant is Infinitus (China) Company , Ltd.. It received FDA 510(k) clearance on 2017-10-23 under 510(k) number K171647. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the BeneLife Premium Facial Treatment Pack, Model: QZ0701A?

BeneLife Premium Facial Treatment Pack, Model: QZ0701A is a medical device that received FDA 510(k) clearance on 2017-10-23. The listed applicant is Infinitus (China) Company , Ltd.. The 510(k) number is K171647.

When did BeneLife Premium Facial Treatment Pack, Model: QZ0701A receive FDA 510(k) clearance?

BeneLife Premium Facial Treatment Pack, Model: QZ0701A received FDA 510(k) clearance on 2017-10-23, under 510(k) number K171647.

Who is the listed applicant for BeneLife Premium Facial Treatment Pack, Model: QZ0701A?

The FDA 510(k) record lists Infinitus (China) Company , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BeneLife Premium Facial Treatment Pack, Model: QZ0701A?

The FDA product code for BeneLife Premium Facial Treatment Pack, Model: QZ0701A is NFO.

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ベネライフプレミアムフェイシャルケアパック、モデル：QZ0701A

医療機器の概要

よくある質問

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