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)

PALMLIGHT 10, MODEL 001-00030

K-Number: K061341 · 2006-06-12

ApplicantCAO Group, Inc.
Decision Date2006-06-12
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PALMLIGHT 10, MODEL 001-00030 is the device name listed in this FDA 510(k) record. The listed applicant is CAO Group, Inc.. It received FDA 510(k) clearance on 2006-06-12 under 510(k) number K061341. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PALMLIGHT 10, MODEL 001-00030?

PALMLIGHT 10, MODEL 001-00030 is a medical device that received FDA 510(k) clearance on 2006-06-12. The listed applicant is CAO Group, Inc.. The 510(k) number is K061341.

When did PALMLIGHT 10, MODEL 001-00030 receive FDA 510(k) clearance?

PALMLIGHT 10, MODEL 001-00030 received FDA 510(k) clearance on 2006-06-12, under 510(k) number K061341.

Who is the listed applicant for PALMLIGHT 10, MODEL 001-00030?

The FDA 510(k) record lists CAO Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PALMLIGHT 10, MODEL 001-00030?

The FDA product code for PALMLIGHT 10, MODEL 001-00030 is EBZ.

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 CAO Group, Inc. 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.

K254197Picasso Pro Diode Laser (002-00460)K201904Monet Curing LaserK201475Ultimate Contour, Ultimate Contour MiniK181602Pioneer Elite Diode LaserK181614Sterling Supreme Diode LaserK181601Precise SHP Diode Laser

View all 27 devices →

Related Devices (Code: EBZ)

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.

K253131Curing Light (M-Cure 6)Guangzhou Rebornendo Medical Instrument Co., Ltd.K253461Demi ProMeta Systems Co., Ltd.K242386BluemoonGenoss Co., Ltd.K243921LED Curing Lights (DB686 HALO)Foshan Coxo Medical Instrument Co., Ltd.K250009LED Curing Light (C01-X, C02-X)Premium Plus (Dongguan) LimitedK241238LOOP™ LED Curing Light System (CLK01)Garrison Dental Solutions, LLC

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.

↑