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FDA 510(k) Applications Submitted by KINETIC INSTRUMENTS, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K022862
08/28/2002
TRANSCURE, MODEL 2910
KINETIC INSTRUMENTS, INC.
K012946
09/04/2001
SUNLITELED MODEL #2810
KINETIC INSTRUMENTS, INC.
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