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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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