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FDA 510(k)

Diode Laser Cap

K-Number: K173678 · 2018-02-28

ApplicantCosmo Far East Technology Limited
Decision Date2018-02-28
Product CodeOAP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Diode Laser Cap is a medical device manufactured by Cosmo Far East Technology Limited. It received FDA 510(k) clearance on 2018-02-28 under approval number K173678. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Diode Laser Cap?

Diode Laser Cap is a medical device that received FDA 510(k) clearance on 2018-02-28. It is manufactured by Cosmo Far East Technology Limited. The 510(k) number is K173678.

When was Diode Laser Cap approved by the FDA?

Diode Laser Cap received FDA 510(k) clearance on 2018-02-28, under approval number K173678.

What company makes Diode Laser Cap?

Diode Laser Cap is manufactured by Cosmo Far East Technology Limited.

What is the FDA product code for Diode Laser Cap?

The FDA product code for Diode Laser Cap is OAP.

Related Clinical Trials

NCT07607028 Comparison of Ultrasonic vs 980-nm Diode Laser Irrigant Activation for Reducing Residual Bacterial DNA in Necrotic Teeth COMPLETED NCT07593508 Diode Laser-Assisted Direct Pulp Capping Trial COMPLETED NCT07278999 Photobiomodulation, Photodynamic Therapy, and Clobetasol in the Treatment of Oral Lichen Planus. RECRUITING NCT07532694 Diode Laser-Assisted Periodontal Therapy in Kidney Transplant Recipients RECRUITING NCT07520266 Gingival Depigmentation With Diode and Er,Cr:YSGG Laser: A Split-mouth Trial COMPLETED NCT05473858 Oraverse Versus Laser RECRUITING

Other Devices by Cosmo Far East Technology Limited

K252325Hair Growth Laser Cap

Related Devices (Code: OAP)

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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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