Oakfield Instruments, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Oakfield Instruments, Ltd. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Oakfield Instruments, Ltd. has 8 FDA 510(k) cleared medical devices. Based in Oxon Ox8 1ja England, GB.
Historical record: 8 cleared submissions from 1989 to 1997. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Oakfield Instruments, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Oakfield Instruments, Ltd.
8 devices
Cleared
Aug 06, 1997
FLEXILOG LS
Gastroenterology & Urology
250d
Cleared
Mar 04, 1997
FLEXILOG 3000
Gastroenterology & Urology
109d
Cleared
Nov 04, 1996
FLEXILOG LS 13921
Gastroenterology & Urology
172d
Cleared
Jun 13, 1995
FLEXILOG 2000
Gastroenterology & Urology
242d
Cleared
Mar 30, 1992
MEDISCINT
Radiology
77d
Cleared
Aug 28, 1990
CARDIOSCINT (LEFT VENTRICULAR FUNCTION MONITOR)
Radiology
85d
Cleared
May 04, 1990
FLEXILOG 1010 AMBULATORY PH MONITORING SYSTEM
Gastroenterology & Urology
186d
Cleared
Oct 17, 1989
SOURCERER
Toxicology
77d