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Silver Bay, LLC
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K112362
C100 WRINKLE REDUCTION DEVICE
August 14, 2012
K111286
QUASAR CALYPSO
January 18, 2012
K091467
BABY QUASAR
September 17, 2010
K093963
QUASAR BLUE LIGHT THERAPY SYSTEM
August 27, 2010
K072767
QUASAR BLUE LIGHT THERAPY SYSTEM
October 15, 2007