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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