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FDA 510(k)

MICROLUX DL

K-Number: K041614 · 2005-04-04

ApplicantAddent, Inc.
Decision Date2005-04-04
Product CodeEAZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MICROLUX DL is the device name listed in this FDA 510(k) record. The listed applicant is Addent, Inc.. It received FDA 510(k) clearance on 2005-04-04 under 510(k) number K041614. The device is classified under product code EAZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROLUX DL?

MICROLUX DL is a medical device that received FDA 510(k) clearance on 2005-04-04. The listed applicant is Addent, Inc.. The 510(k) number is K041614.

When did MICROLUX DL receive FDA 510(k) clearance?

MICROLUX DL received FDA 510(k) clearance on 2005-04-04, under 510(k) number K041614.

Who is the listed applicant for MICROLUX DL?

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

What is the FDA product code for MICROLUX DL?

The FDA product code for MICROLUX DL is EAZ.

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.

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Other records listing Addent, 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.

K182017Compex HDK121282MICROLUX/DL MICROLUX/BLU BIO/SCREENK082668BIO-SCREENK072309MICROLUX/BLUK062961MICROLUX TRANSILLUMINATORK061395CALSET COMPOSITE HEATER

View all 7 devices →

Related Devices (Code: EAZ)

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.

K072309MICROLUX/BLUAddent, Inc.K033033VIZILITE-BLUE ORAL EXAM KITTrylon Corp.K003995SPECULITE/ORALLITETrylon Corp.K926081DENTAL LIGHTMdt Corp., Inc.K935390SIROLUX FANTASTICPelton & Crane Co.K925629ACCESSORY TO IMPROVED DENTAL OPERATING LIGHTDen-Tal-Ez Mfg Co., Inc.

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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