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FDA 510(k)

LightLas Multi-Wavelength Medical Laser System

K-Number: K152688 · 2016-06-15

ApplicantLightmed Corporation
Decision Date2016-06-15
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LightLas Multi-Wavelength Medical Laser System is a medical device manufactured by Lightmed Corporation. It received FDA 510(k) clearance on 2016-06-15 under approval number K152688. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LightLas Multi-Wavelength Medical Laser System?

LightLas Multi-Wavelength Medical Laser System is a medical device that received FDA 510(k) clearance on 2016-06-15. It is manufactured by Lightmed Corporation. The 510(k) number is K152688.

When was LightLas Multi-Wavelength Medical Laser System approved by the FDA?

LightLas Multi-Wavelength Medical Laser System received FDA 510(k) clearance on 2016-06-15, under approval number K152688.

What company makes LightLas Multi-Wavelength Medical Laser System?

LightLas Multi-Wavelength Medical Laser System is manufactured by Lightmed Corporation.

What is the FDA product code for LightLas Multi-Wavelength Medical Laser System?

The FDA product code for LightLas Multi-Wavelength Medical Laser System is HQF.

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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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