ClearanceBrief
Company ยท US

Oxford Instruments, Plc.

FDA 510(k) clearances and medical device recalls filed under this name, 1994 to 2001. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
HELMonitor, Heart Rate, Fetal, Ultrasonic2
DQKComputer, Diagnostic, Programmable1
GWFStimulator, Electrical, Evoked Response1
GWQFull-Montage Standard Electroencephalograph1
HGMSystem, Monitoring, Perinatal1
OLZAutomatic Event Detection Software For Polysomnograph With Electroencephalograph1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 9, 2001K002150SONICAID FM820, SONICAID FM830
Oxford Instruments, GB
HGM
Sep 13, 2000K002544MEDILOG EXCEL 2 - HOLTER MANAGEMENT SYSTEM
Oxford Instruments, GB
DQK
Jul 16, 1998K981405SYNERGY LT
Oxford Instruments, Plc., GB
GWF
Jan 17, 1997K961642MEDILOG MR95
Oxford Instruments, Plc.
GWQ
Jan 17, 1997K961636MEDILOG VISION
Oxford Instruments, Plc.
OLZ
Aug 24, 1995K930714SONICAID MODEL TEAM FECG IUP
Oxford Instruments, Plc.
HEL
Dec 22, 1994K933816SONICAID MODEL P110 FETAL HEAR DETECTOR
Oxford Instruments, Plc.
HEL

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes