FDA 510(k) Applications Submitted by BOB DUFFY
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K150304 | 02/06/2015 | Oxyless Blood Tubing Set | Oxyless Ltd |
| K120560 | 02/24/2012 | TRINITY WRINKLE REMOVER | Carol Cole Company |
| K103472 | 11/24/2010 | NUFACE PLUS | Carol Cole Company |
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