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FDA 510(k) Applications Submitted by KENNETH J KISCO
FDA 510(k) Number
Submission Date
Device Name
Applicant
K964400
11/04/1996
ALPHATEC EXTERNAL FIXATION SYSTEM
ALPHATEC MFG., INC.
K955355
11/21/1995
VARIANT ALPHA-THALASSEMIA SHORT PROGRAM
BIO-RAD
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