Atlas FDA

SONX 35 ULTRASONIC BLEACHING SYSTEM; SONIWHITE ULTRA SONIC, MODEL QUICK WHITE US

FDA 510(k) clearance K041392 · decided 2004-11-08

Clearance details

K-number
K041392
Device name
SONX 35 ULTRASONIC BLEACHING SYSTEM; SONIWHITE ULTRA SONIC, MODEL QUICK WHITE US
Applicant
CAO Group, Inc.
Decision
Substantially Equivalent
Date received
2004-05-25
Decision date
2004-11-08
Days to decision
167 days
Clearance type
Traditional
Product code
EEG
Device class
1
Regulation number
872.6475
Medical specialty
Dental
Advisory committee
Dental
Location
Sandy, UT, US
Third-party review
No
Expedited review
No

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SCHEIN BLEACHING UNIT (K862385)Henry Schein, Inc.1986-10-30
MONARCH II BLEACHING INSTRUMENT (K854692)Almore Intl., Inc.1986-05-12
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.