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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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