Atlas FDA

MONARCH II BLEACHING INSTRUMENT

FDA 510(k) clearance K854692 · decided 1986-05-12

Clearance details

K-number
K854692
Device name
MONARCH II BLEACHING INSTRUMENT
Applicant
Almore Intl., Inc.
Decision
Substantially Equivalent
Date received
1985-11-21
Decision date
1986-05-12
Days to decision
172 days
Clearance type
Traditional
Product code
EEG
Device class
1
Regulation number
872.6475
Medical specialty
Dental
Advisory committee
Dental
Location
Portland, OR, 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
TANDA PEARL, ULTRAWYTE, PEARL (K122725)Syneron Beauty2012-11-27
ABSOLUTE WHITE LIGHT (K110888)Dr. Fresh, Inc.2012-01-12
BRITEWHITE TEETH WHITENING SYSTEM, MODEL BW1101 (K063704)Beks Incorporated2007-02-20
QUICKSMILE (K052040)Cosmetic Dental Materials, Inc.2005-10-18
SOUTH BEACH SMILE LIGHT WHITENING SYSTEM (K042153)Dentovations, Inc.2004-11-08
SONX 35 ULTRASONIC BLEACHING SYSTEM; SONIWHITE ULTRA SONIC, MODEL QUICK WHITE US (K041392)CAO Group, Inc.2004-11-08
UNION BROACH BLEACHING LIGHT (K895174)Union Broach, Div. Moyco Industries, Inc.1990-04-13
BEEHIVE-64 OR BEEHIVE-32, DIGITAL EEG RECORDING (K884937)Grass-Telefactor Product Group1989-04-14
SCHEIN BLEACHING UNIT (K862385)Henry Schein, Inc.1986-10-30
HOT PROBE MODEL 6001 (K832179)Analytic Technology1983-10-04
REYNOLDS BLEACHING PROCESS (K790378)Reynolds Laboratories1979-04-10

Recalls involving this device

No recalls on record reference this clearance.