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. 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.
Related Devices (Code: NFO)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.