FDA 510(k) Applications Submitted by SILVERBAY LLC, D/B/A QUASAR BIO-TECH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K130225 | 01/29/2013 | QUASAR C100, BABY QUASAR PLUS, QUASAR MD PLUS; WRINKLE REDUCTION DEVICE | SILVERBAY LLC, D/B/A QUASAR BIO-TECH |
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