FDA 510(k) Applications Submitted by AXON INSTRUMENTS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K990683 03/03/1999 AXON MP-1 MICROPOSITIONER AXON INSTRUMENTS, INC.
K970943 03/14/1997 GUIDELINE SYSTEM AXON INSTRUMENTS, INC.
K971318 04/09/1997 MM-1 MOVEMENT MONITOR AXON INSTRUMENTS, INC.


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