FDA 510(k) Applications Submitted by THOMAS A BOONE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K980379 | 01/30/1998 | PROWESS PRO-SIM | SSGI PROWESS SYSTEMS |
| K073450 | 12/10/2007 | SUTTER ELECTROSURGICAL CABLES | SUTTER MEDIZINTECHNIK GMBH |
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