FDA 510(k) Applications Submitted by TIMOTHY LEE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K100100 | 01/12/2010 | DIO STEADY EXTERNAL IMPLANT SYSTEM | DIO CORPORATION |
| K122519 | 08/17/2012 | DIO UF HSA INTERNAL SUB-MERGED IMPLANT SYSTEM | DIO CORPORATION |
| K112746 | 09/21/2011 | DIOSLIMON IMPLANT SYSTEM | DIO CORPORATION |
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