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FDA 510(k)

POWER LED

K-Number: K033697 · 2004-02-27

ApplicantDental Products of USA, Inc.
Decision Date2004-02-27
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

POWER LED is the device name listed in this FDA 510(k) record. The listed applicant is Dental Products of USA, Inc.. It received FDA 510(k) clearance on 2004-02-27 under 510(k) number K033697. 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 POWER LED?

POWER LED is a medical device that received FDA 510(k) clearance on 2004-02-27. The listed applicant is Dental Products of USA, Inc.. The 510(k) number is K033697.

When did POWER LED receive FDA 510(k) clearance?

POWER LED received FDA 510(k) clearance on 2004-02-27, under 510(k) number K033697.

Who is the listed applicant for POWER LED?

The FDA 510(k) record lists Dental Products of USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWER LED?

The FDA product code for POWER LED is EBZ.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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