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FDA 510(k)

MICROLUX/BLU

K-Number: K072309 · 2007-11-19

ApplicantAddent, Inc.
Decision Date2007-11-19
Product CodeEAZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MICROLUX/BLU is the device name listed in this FDA 510(k) record. The listed applicant is Addent, Inc.. It received FDA 510(k) clearance on 2007-11-19 under 510(k) number K072309. 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/BLU?

MICROLUX/BLU is a medical device that received FDA 510(k) clearance on 2007-11-19. The listed applicant is Addent, Inc.. The 510(k) number is K072309.

When did MICROLUX/BLU receive FDA 510(k) clearance?

MICROLUX/BLU received FDA 510(k) clearance on 2007-11-19, under 510(k) number K072309.

Who is the listed applicant for MICROLUX/BLU?

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/BLU?

The FDA product code for MICROLUX/BLU 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-SCREENK062961MICROLUX TRANSILLUMINATORK061395CALSET COMPOSITE HEATERK041614MICROLUX DL

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.

K041614MICROLUX DLAddent, 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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