Atlas FDA

TANDA PEARL, ULTRAWYTE, PEARL

FDA 510(k) clearance K122725 · decided 2012-11-27

Clearance details

K-number
K122725
Device name
TANDA PEARL, ULTRAWYTE, PEARL
Applicant
Syneron Beauty
Decision
Substantially Equivalent
Date received
2012-09-05
Decision date
2012-11-27
Days to decision
83 days
Clearance type
Traditional
Product code
EEG
Device class
1
Regulation number
872.6475
Medical specialty
Dental
Advisory committee
Dental
Location
Philedelphia, PA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.