FDA 510(k) Applications Submitted by NEURO VASX, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K011646 05/29/2001 NEUROEDGE INFUSION CATHETER NEURO VASX, INC.
K984258 11/30/1998 NEUROVASX SUB-MICROINFUSION CATHETER NEURO VASX, INC.


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