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)

IPL Therapy Machine

K-Number: K161286 · 2016-08-04

Decision Date2016-08-04
Product CodeONF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IPL Therapy Machine is a medical device manufactured by Beijing Adss Development Co., Ltd.. It received FDA 510(k) clearance on 2016-08-04 under approval number K161286. The device is classified under product code ONF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IPL Therapy Machine?

IPL Therapy Machine is a medical device that received FDA 510(k) clearance on 2016-08-04. It is manufactured by Beijing Adss Development Co., Ltd.. The 510(k) number is K161286.

When was IPL Therapy Machine approved by the FDA?

IPL Therapy Machine received FDA 510(k) clearance on 2016-08-04, under approval number K161286.

What company makes IPL Therapy Machine?

IPL Therapy Machine is manufactured by Beijing Adss Development Co., Ltd..

What is the FDA product code for IPL Therapy Machine?

The FDA product code for IPL Therapy Machine is ONF.

Related Clinical Trials

Related PubMed Literature

Other Devices by Beijing Adss Development Co., Ltd.

View all 10 devices →

Related Devices (Code: ONF)

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.