FDA 510(k) Applications Submitted by SANTA SUNDELL
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K993588 | 10/22/1999 | MODIFICATION TO RX HERCULINK 14 BILIARY STENT SYSTEM, MODELS 1005126-13, 1005128-13, 1005130-13, 1005132-13, 1005134-13, | GUIDANT CORP. |
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