Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LIGHTLAS SELECTOR

K-Number: K090774 · 2009-08-13

ApplicantLightmed Corp.
Decision Date2009-08-13
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LIGHTLAS SELECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Lightmed Corp.. It received FDA 510(k) clearance on 2009-08-13 under 510(k) number K090774. 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 SELECTOR?

LIGHTLAS SELECTOR is a medical device that received FDA 510(k) clearance on 2009-08-13. The listed applicant is Lightmed Corp.. The 510(k) number is K090774.

When did LIGHTLAS SELECTOR receive FDA 510(k) clearance?

LIGHTLAS SELECTOR received FDA 510(k) clearance on 2009-08-13, under 510(k) number K090774.

Who is the listed applicant for LIGHTLAS SELECTOR?

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 SELECTOR?

The FDA product code for LIGHTLAS SELECTOR is HQF.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 SYSTEMK091981LIGHTLAS 577 MEDICAL OPTICAL PUMPED SEMICONDUCTOR LASERK091534LIGHTLAS MODEL 532K063297LIGHTLAS 561 OPTHALMIC PHOTOCOAGULATORK021538LIGHTLAS 810 INFRARED LASER PHOTOCOAGULATOR

View all 8 devices →

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.

↑