FDA 510(k) Applications Submitted by KRISTINE LIBERACKI

FDA 510(k) Number Submission Date Device Name Applicant
K050873 04/06/2005 CANALIZER HYDROPHILIC GUIDE WIRE MEDICAL DEVICE TECHNOLOGIES, INC.
K051421 06/01/2005 INTER V BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR MEDICAL DEVICE TECHNOLOGIES, INC.
K053518 12/19/2005 INTERV BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR MEDICAL DEVICE TECHNOLOGIES, INC.


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