FDA 510(k) Applications Submitted by WILLIAM J BECKER
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K022862 | 08/28/2002 | TRANSCURE, MODEL 2910 | KINETIC INSTRUMENTS, INC. |
| K012946 | 09/04/2001 | SUNLITELED MODEL #2810 | KINETIC INSTRUMENTS, INC. |
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