FDA 510(k) Applications Submitted by SILVER BAY, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K091467 | 05/18/2009 | BABY QUASAR | SILVER BAY, LLC |
| K072767 | 09/28/2007 | QUASAR BLUE LIGHT THERAPY SYSTEM | SILVER BAY, LLC |
| K093963 | 12/23/2009 | QUASAR BLUE LIGHT THERAPY SYSTEM | SILVER BAY, LLC |
| K111286 | 05/06/2011 | QUASAR CALYPSO | SILVER BAY, LLC |
| K112362 | 08/17/2011 | C100 WRINKLE REDUCTION DEVICE | SILVER BAY, LLC |
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