FDA 510(k) Applications Submitted by PRO-MED INSTRUMENTS GMBH

FDA 510(k) Number Submission Date Device Name Applicant
K001808 06/15/2000 DORO HEADREST SYSTEM PRO-MED INSTRUMENTS GMBH
K070997 04/09/2007 DORO NON-STICK BIPOLAR FORCEPS, MODEL 5001-XX TO 5012-XX, DORO BIPOLAR REUSABLE CABLES, MODEL 5015-XX PRO-MED INSTRUMENTS GMBH
K063494 11/20/2006 DORO RADIOLUCENT HEADREST SYSTEM ( ALSO MRI-COMPATIBLE) AND COMPONENTS PRO-MED INSTRUMENTS GMBH
K032331 07/29/2003 DORO RADIOLUCENT HEADREST SYSTEM AND HORSESHOE HEADRESTS,AND NON-RADIOLUCENT J-ARM RETRACTOR SYSTEM (ALUMINUM ALLOY) PRO-MED INSTRUMENTS GMBH


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