FDA 510(k) Applications Submitted by DAVID L REGAN

FDA 510(k) Number Submission Date Device Name Applicant
K031091 04/07/2003 VTI 20 MHZ GATED DOPPLER VASCULAR TECHNOLOGY INCORPORATED
K002990 09/25/2000 VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000; VTI SKULL SCREW, MODEL 22001 VASCULAR TECHNOLOGY INCORPORATED
K082870 09/29/2008 VTI INTRAOPERATIVE DOPPLER SYSTEMS VASCULAR TECHNOLOGY INCORPORATED


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