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FDA 510(k)

Handheld Diode Laser for Hair Removal

K-Number: K163173 · 2017-02-08

ApplicantLiaoning Sidey Optoelectronics Technologies Co., Ltd.
Decision Date2017-02-08
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Handheld Diode Laser for Hair Removal is a medical device manufactured by Liaoning Sidey Optoelectronics Technologies Co., Ltd.. It received FDA 510(k) clearance on 2017-02-08 under approval number K163173. 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 Handheld Diode Laser for Hair Removal?

Handheld Diode Laser for Hair Removal is a medical device that received FDA 510(k) clearance on 2017-02-08. It is manufactured by Liaoning Sidey Optoelectronics Technologies Co., Ltd.. The 510(k) number is K163173.

When was Handheld Diode Laser for Hair Removal approved by the FDA?

Handheld Diode Laser for Hair Removal received FDA 510(k) clearance on 2017-02-08, under approval number K163173.

What company makes Handheld Diode Laser for Hair Removal?

Handheld Diode Laser for Hair Removal is manufactured by Liaoning Sidey Optoelectronics Technologies Co., Ltd..

What is the FDA product code for Handheld Diode Laser for Hair Removal?

The FDA product code for Handheld Diode Laser for Hair Removal is OHT.

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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.

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