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 Hair removal

K-Number: K203510 · 2021-02-26

Decision Date2021-02-26
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IPL Hair removal is a medical device manufactured by Shenzhen Weikai Technology Co.,Ltd. It received FDA 510(k) clearance on 2021-02-26 under approval number K203510. The device is classified under product code OHT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IPL Hair removal?

IPL Hair removal is a medical device that received FDA 510(k) clearance on 2021-02-26. It is manufactured by Shenzhen Weikai Technology Co.,Ltd. The 510(k) number is K203510.

When was IPL Hair removal approved by the FDA?

IPL Hair removal received FDA 510(k) clearance on 2021-02-26, under approval number K203510.

What company makes IPL Hair removal?

IPL Hair removal is manufactured by Shenzhen Weikai Technology Co.,Ltd.

What is the FDA product code for IPL Hair removal?

The FDA product code for IPL Hair removal is OHT.

Related Devices (Code: OHT)

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.