FDA 510(k) Applications Submitted by VENTREX, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K061044 04/14/2006 FEATHERLITE AQUA TOCODYNAMOMETER VENTREX, INC.
K013477 10/19/2001 TOCO LITE, MODEL TD-01 VENTREX, INC.
K964821 12/02/1996 COVEROX SHEATH MODELS NUMBER PS65, PS67, EPS65 AND EPS67 VENTREX, INC.


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