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FDA 510(k)

Myolight Microcurrent Handpiece

K-Number: K243063 · 2025-02-10

Decision Date2025-02-10
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Myolight Microcurrent Handpiece is a medical device manufactured by Raja Trading Company, Inc.. It received FDA 510(k) clearance on 2025-02-10 under approval number K243063. 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 Myolight Microcurrent Handpiece?

Myolight Microcurrent Handpiece is a medical device that received FDA 510(k) clearance on 2025-02-10. It is manufactured by Raja Trading Company, Inc.. The 510(k) number is K243063.

When was Myolight Microcurrent Handpiece approved by the FDA?

Myolight Microcurrent Handpiece received FDA 510(k) clearance on 2025-02-10, under approval number K243063.

What company makes Myolight Microcurrent Handpiece?

Myolight Microcurrent Handpiece is manufactured by Raja Trading Company, Inc..

What is the FDA product code for Myolight Microcurrent Handpiece?

The FDA product code for Myolight Microcurrent Handpiece is NFO.

Other Devices by Raja Trading Company, Inc.

Related Devices (Code: NFO)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.