FDA 510(k) Applications Submitted by TAMIMA ITANI, PH.D.

FDA 510(k) Number Submission Date Device Name Applicant
K001220 04/17/2000 ENDOPATH SURESEAL REDUCER CAP ETHICON ENDO-SURGERY, INC.
K991980 06/14/1999 MAMMOTOME HH HAND-HELD PROBE, VACUUM SET, CONTROL MODULE, HH HAND-HELD HOLSTER AND CABLES, SOFTWARE PACKAGE, FOOTSWITCH, ETHICON ENDO-SURGERY, INC.
K992813 08/20/1999 11 GAUGE PROBE, STEREOTACTIC, 14 GAUGE PROBE, STEREOTACTIC,14 GAUGE PROBE, ULTRASOUND, HOUSING STEREOTACTIC,HOUSING, ULT ETHICON ENDO-SURGERY, INC.
K973654 09/25/1997 VIAL-MATE RECONSTITUTION DEVICE (2B8071) BAXTER HEALTHCARE CORP.
K961703 05/02/1996 COLLEAGUE 2 VOLUMETRIC INFUSION PUMP(DUAL CHANNEL)/COLLEAGUE 3 VOLUMETRIC INFUSION PUMP(TREE CHANNEL) BAXTER HEALTHCARE CORP.


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