Atlas FDA

MICROLUX DL

FDA 510(k) clearance K041614 · decided 2005-04-04

Clearance details

K-number
K041614
Device name
MICROLUX DL
Applicant
Addent, Inc.
Decision
Substantially Equivalent
Date received
2004-06-15
Decision date
2005-04-04
Days to decision
293 days
Clearance type
Traditional
Product code
EAZ
Device class
1
Regulation number
872.4630
Medical specialty
Dental
Advisory committee
Dental
Location
Danbury, CT, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
MICROLUX/BLU (K072309)Addent, Inc.2007-11-19
VIZILITE-BLUE ORAL EXAM KIT (K033033)Trylon Corp.2004-11-22
SPECULITE/ORALLITE (K003995)Trylon Corp.2001-03-16
DENTAL LIGHT (K926081)Mdt Corp., Inc.1994-01-26
SIROLUX FANTASTIC (K935390)Pelton & Crane Co.1993-12-10
ACCESSORY TO IMPROVED DENTAL OPERATING LIGHT (K925629)Den-Tal-Ez Mfg Co., Inc.1993-11-23
DELIGHT (K923462)Planmeca USA, Inc.1992-12-21
MICRONAIRE ISO-HOOD MAX 5UV (K912142)Micronaire Corp.1991-10-30
MINIFLEX AND PERSONAL UNIT (K912997)Dabi-Atlante America Corp.1991-10-30
DEFIANCE MODEL FUS 336 (K902685)Defiance Electronics, Inc.1990-09-17
ISOLIGHT (K894059)Eurodent, Inc.1989-09-07
A-DEC DENTAL LIGHT (K893044)A-Dec, Inc.1989-07-14

Recalls involving this device

No recalls on record reference this clearance.