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FDA 510(k)

LightLas Multi-Wavelength Medical Laser System

K-Number: K152688 · 2016-06-15

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

Device Summary

LightLas Multi-Wavelength Medical Laser System is the device name listed in this FDA 510(k) record. The listed applicant is Lightmed Corporation. It received FDA 510(k) clearance on 2016-06-15 under 510(k) 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. The listed applicant is Lightmed Corporation. The 510(k) number is K152688.

When did LightLas Multi-Wavelength Medical Laser System receive FDA 510(k) clearance?

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

Who is the listed applicant for LightLas Multi-Wavelength Medical Laser System?

The FDA 510(k) record lists Lightmed Corporation as the applicant. This does not by itself establish the device manufacturer.

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.

Related Devices (Code: HQF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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