FDA 510(k) Applications Submitted by VASCON LLC

FDA 510(k) Number Submission Date Device Name Applicant
K052004 07/25/2005 VASCON NEUROPATH GUIDING CATHETER VASCON LLC
K033633 11/19/2003 VASCON POLARIS GUIDING CATHETER VASCON LLC
K053310 11/28/2005 VASCON ROAMER MICROCATHETER VASCON LLC
K043387 12/09/2004 VASCON POLARIS GUIDING CATHETER VASCON LLC


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