Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BeneLife Premium Facial Treatment Pack, Model: QZ0701A

K-Number: K171647 · 2017-10-23

Decision Date2017-10-23
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

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

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.

Related Clinical Trials

Related PubMed Literature

Related Devices (Code: NFO)

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.