FDA 510(k) Applications Submitted by ANITA THIBEAULT
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K001808 | 06/15/2000 | DORO HEADREST SYSTEM | PRO-MED INSTRUMENTS GMBH |
| K992760 | 08/17/1999 | SELECT-SUTTER MICRO BIPOLAR FORCEPS | SELECT MEDIZINTECHNIK HERMANN SUTTER GMBH |
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