FDA 510(k) Applications Submitted by OXFORD INSTRUMENTS, PLC.

FDA 510(k) Number Submission Date Device Name Applicant
K961636 04/29/1996 MEDILOG VISION OXFORD INSTRUMENTS, PLC.
K961642 04/29/1996 MEDILOG MR95 OXFORD INSTRUMENTS, PLC.
K981405 04/20/1998 SYNERGY LT OXFORD INSTRUMENTS, PLC.


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