Oxford Instruments, Plc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K002150SONICAID FM820, SONICAID FM830March 9, 2001
K002544MEDILOG EXCEL 2 - HOLTER MANAGEMENT SYSTEMSeptember 13, 2000
K981405SYNERGY LTJuly 16, 1998
K961642MEDILOG MR95January 17, 1997
K961636MEDILOG VISIONJanuary 17, 1997
K930714SONICAID MODEL TEAM FECG IUPAugust 24, 1995
K933816SONICAID MODEL P110 FETAL HEAR DETECTORDecember 22, 1994