Oxford Medilog, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
48
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K923737MODEL MEDILOG RAPIDEJanuary 5, 1994
K920295MEDILOG EXCEL ECG ANALYSIS SYSTEM (MODIFIED)August 18, 1992
K912890MODEL SONICAID AXISJanuary 9, 1992
K912639SONICAID TEAMDecember 31, 1991
K904763MENTOR EEG SYSTEMApril 10, 1991
K902690SONICAID MODEL MERIDIAN 800February 5, 1991
K895909SONICAID MODEL VASOFLO 4July 9, 1990
K896535MEDILOG OPTIMAJanuary 18, 1990
K891383MEDILOG 9200 EEG REPLAY/ANALYSIS SYSTEMJune 1, 1989
K890330MEDILOG 6000-FD REPORT GENERATORApril 20, 1989
K890338MEDILOG EDITORApril 19, 1989
K890647MEDILOG 9000-II AMBULATORY RECORDERMarch 15, 1989
K874917PYTHON AMBULATORY BLOOD PRESSURE MONITORING SYSTEMMay 10, 1988
K873680MODEL 6000FD AMBULATORY ECG ANALYSIS SYSTEMNovember 23, 1987
K871990MODEL MPA MULTI PARAMETER ANALYSIS MONITORING SYS.October 7, 1987
K872497MODEL MR-45 AMBULATORY HOLTER MONITOROctober 6, 1987
K871500MODEL 5000 AMBULATORY MONITORING SYSTEMJuly 1, 1987
K863724MODEL 6000 AMBULATORY ECG ANALYSIS SYSTEMNovember 20, 1986
K862536MODEL 1010 AMBULATORY PH MONITORING SYSTEMSeptember 12, 1986
K860458ELECTROPHYSIOLOGICAL SYSTEM TO MONITOR SKIN TEMP.August 12, 1986