Oxford Instruments, Plc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oxford Instruments, Plc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Oxford Instruments, Plc. has 5 FDA 510(k) cleared medical devices. Based in Clearwater, US.
Historical record: 5 cleared submissions from 1994 to 1998. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Oxford Instruments, Plc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Oxford Instruments, Plc.
5 devices
Cleared
Jul 16, 1998
SYNERGY LT
Neurology
87d
Cleared
Jan 17, 1997
MEDILOG VISION
Neurology
263d
Cleared
Jan 17, 1997
MEDILOG MR95
Neurology
263d
Cleared
Aug 24, 1995
SONICAID MODEL TEAM FECG IUP
Obstetrics & Gynecology
924d
Cleared
Dec 22, 1994
SONICAID MODEL P110 FETAL HEAR DETECTOR
Obstetrics & Gynecology
505d