Company ยท GB
Oakfield Instruments, Ltd.
FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 1997. Name variants (Inc, Corp, punctuation) are merged.
8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 6, 1997 | K964804 | FLEXILOG LS Oakfield Instruments, Ltd., GB | KLA |
| Mar 4, 1997 | K964589 | FLEXILOG 3000 Oakfield Instruments, Ltd., GB | KLA |
| Nov 4, 1996 | K961895 | FLEXILOG LS 13921 Oakfield Instruments, Ltd., GB | KLA |
| Jun 13, 1995 | K945069 | FLEXILOG 2000 Oakfield Instruments, Ltd., GB | FFT |
| Mar 30, 1992 | K920115 | MEDISCINT Oakfield Instruments, Ltd., GB | IZD |
| Aug 28, 1990 | K902460 | CARDIOSCINT (LEFT VENTRICULAR FUNCTION MONITOR) Oakfield Instruments, Ltd., GB | IZD |
| May 4, 1990 | K896288 | FLEXILOG 1010 AMBULATORY PH MONITORING SYSTEM Oakfield Instruments, Ltd., GB | FFT |
| Oct 17, 1989 | K894902 | SOURCERER Oakfield Instruments, Ltd., GB | JJJ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||