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FDA 510(k)

LIGHTLAS 577 MEDICAL OPTICAL PUMPED SEMICONDUCTOR LASER

K-Number: K091981 · 2009-09-28

ApplicantLightmed Corp.
Decision Date2009-09-28
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LIGHTLAS 577 MEDICAL OPTICAL PUMPED SEMICONDUCTOR LASER is the device name listed in this FDA 510(k) record. The listed applicant is Lightmed Corp.. It received FDA 510(k) clearance on 2009-09-28 under 510(k) number K091981. 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 577 MEDICAL OPTICAL PUMPED SEMICONDUCTOR LASER?

LIGHTLAS 577 MEDICAL OPTICAL PUMPED SEMICONDUCTOR LASER is a medical device that received FDA 510(k) clearance on 2009-09-28. The listed applicant is Lightmed Corp.. The 510(k) number is K091981.

When did LIGHTLAS 577 MEDICAL OPTICAL PUMPED SEMICONDUCTOR LASER receive FDA 510(k) clearance?

LIGHTLAS 577 MEDICAL OPTICAL PUMPED SEMICONDUCTOR LASER received FDA 510(k) clearance on 2009-09-28, under 510(k) number K091981.

Who is the listed applicant for LIGHTLAS 577 MEDICAL OPTICAL PUMPED SEMICONDUCTOR LASER?

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 577 MEDICAL OPTICAL PUMPED SEMICONDUCTOR LASER?

The FDA product code for LIGHTLAS 577 MEDICAL OPTICAL PUMPED SEMICONDUCTOR LASER 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 SYSTEMK103547LIGHTLAS MULTI-WAVELENGTH MEDICAL LASER SYSTEMK091534LIGHTLAS 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.

K252979Voyager DSLT (430840610)Belkin Vision, Ltd.K251507INTEGRE LIOQuantel MedicalK251772Navilas Laser System 577sl (156691)Od-Os GmbHK243014EyeQ nanoECPEyeq, Inc.K240615Leos Laser and Endoscopy SystemBeaver-Visitec International, Inc.K242397LYNX PhotocoagulatorNorlase Aps

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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