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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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