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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