Oakfield Instruments, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K964804 | FLEXILOG LS | August 6, 1997 |
| K964589 | FLEXILOG 3000 | March 4, 1997 |
| K961895 | FLEXILOG LS 13921 | November 4, 1996 |
| K945069 | FLEXILOG 2000 | June 13, 1995 |
| K920115 | MEDISCINT | March 30, 1992 |
| K902460 | CARDIOSCINT (LEFT VENTRICULAR FUNCTION MONITOR) | August 28, 1990 |
| K896288 | FLEXILOG 1010 AMBULATORY PH MONITORING SYSTEM | May 4, 1990 |
| K894902 | SOURCERER | October 17, 1989 |