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FDA 510(k) Applications Submitted by OAKFIELD INSTRUMENTS, LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K961895
05/16/1996
FLEXILOG LS 13921
OAKFIELD INSTRUMENTS, LTD.
K964589
11/15/1996
FLEXILOG 3000
OAKFIELD INSTRUMENTS, LTD.
K964804
11/29/1996
FLEXILOG LS
OAKFIELD INSTRUMENTS, LTD.
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