FDA 510(k) Applications Submitted by MATT WILKEN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960080 | 01/11/1996 | ACCUTEMP PROBE | KENTEC MEDICAL, INC. |
| K970686 | 02/25/1997 | ACCUTEMP-PROBE | KENTEC MEDICAL, INC. |
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