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FDA 510(k)

LIGHTLAS MULTI-WAVELENGTH MEDICAL LASER SYSTEM

K-Number: K103547 · 2011-11-03

ApplicantLightmed Corp.
Decision Date2011-11-03
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 Corp.. It received FDA 510(k) clearance on 2011-11-03 under 510(k) number K103547. 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 2011-11-03. The listed applicant is Lightmed Corp.. The 510(k) number is K103547.

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 2011-11-03, under 510(k) number K103547.

Who is the listed applicant for LIGHTLAS MULTI-WAVELENGTH MEDICAL LASER SYSTEM?

The FDA 510(k) record lists Lightmed Corp. 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.

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Other records listing Lightmed Corp. as applicant

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.

K124043LIGHTLAS FAMILY OF MULTI-WAVELENGTH MEDICAL LASER SYSTEMK091981LIGHTLAS 577 MEDICAL OPTICAL PUMPED SEMICONDUCTOR LASERK091534LIGHTLAS MODEL 532K090774LIGHTLAS SELECTORK063297LIGHTLAS 561 OPTHALMIC PHOTOCOAGULATORK021538LIGHTLAS 810 INFRARED LASER PHOTOCOAGULATOR

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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.

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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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