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FDA 510(k) Applications Submitted by ROBERT GUTHRIE
FDA 510(k) Number
Submission Date
Device Name
Applicant
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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