FDA 510(k) Applications Submitted by VELOCIMED INC.

FDA 510(k) Number Submission Date Device Name Applicant
K042117 08/05/2004 PROXIS SYSTEM, MODEL EPS 101 VELOCIMED INC.
K042910 10/21/2004 VENTURE WIRE CONTROL CATHETER, MODEL WCC VELOCIMED INC.
K043084 11/08/2004 PREMERE DELIVERY SHEATH, MODEL PDS VELOCIMED INC.
K052523 09/14/2005 PROXIS SYSTEM VELOCIMED INC.
K040922 04/08/2004 VENTURE WIRE CONTROL CATHETER VELOCIMED INC.


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