FDA 510(k) Applications Submitted by DEAN KNIGHT
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K110687 | 03/11/2011 | RELIEVA STRATUS PRO MICROFLOW SPACER (FRONTAL) | ACCLARENT, INC. |
| K001258 | 04/18/2000 | BX TRANSHEPATIC BILIARY STENT AND DELIVERY SYSTEM | CORDIS CORP. |
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