BeneLife Premium Facial Treatment Pack, Model: QZ0701A
K-Number: K171647 · 2017-10-23
Device Summary
Frequently Asked Questions
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. It is manufactured by Infinitus (China) Company , Ltd.. The 510(k) number is K171647.
When was BeneLife Premium Facial Treatment Pack, Model: QZ0701A approved by the FDA?
BeneLife Premium Facial Treatment Pack, Model: QZ0701A received FDA 510(k) clearance on 2017-10-23, under approval number K171647.
What company makes BeneLife Premium Facial Treatment Pack, Model: QZ0701A?
BeneLife Premium Facial Treatment Pack, Model: QZ0701A is manufactured by Infinitus (China) Company , Ltd..
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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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.