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FDA 510(k) Applications Submitted by ROBERT BRUCE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K982927
08/20/1998
QUICK TAP SELF DRILLING SCREW
KINAMED, INC.
K964362
11/01/1996
KINAMED PROFIX SYSTEM
KINAMED, INC.
K002457
08/10/2000
!NSURE FECAL OCCULT BLOOD TEST
ENTERIX INC.
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