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Kinetic Instruments, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K022862 TRANSCURE, MODEL 2910EBZ2002-10-18 View
510(k) K012946 SUNLITELED MODEL #2810EBZ2001-10-02 View
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