Home / Companies / Invivo Research, Inc.

Invivo Research, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K050399MRI COMPATIBLE PATIENT MONITORING SYSTEM, MODEL 3160August 26, 2005
K043354MODULAR TELEMETRY SYSTEM FOR THE VISION TELEPAK, MODEL 20701January 10, 2005
K041918INTEGRATED PATIENT MONITORING SYSTEMOctober 15, 2004
K040915MAGNITUDE 3150M MRI PATIENT MONITOR, MODEL 3150MSeptember 22, 2004
K002604CENTURION 2000 CENTRAL STATION ARRHYTHMIA PATIENT MONITORING SYSTEMFebruary 7, 2002
K002030OMNI-TRAK 3150/3155A SERIES MONITOR WITH ANESTHETIC AGENT, MODEL 3155A SERIESSeptember 26, 2000
K980045CENTURION CENTRAL STATION ARRHYTHMIA PATIENT MONITORING SYSTEMNovember 16, 1998
K974581MILLENNIA 3500 SERIES MONITOR WITH ANTHESTHETIC AGENTOctober 28, 1998
K971840OMNI-TRAK MODEL 3150 SERIES PATIENT MONITORING SYSTEMMarch 4, 1998
K955045OMNI-TRAK PATIENT MONITORING SYSTEMJuly 11, 1996
K945138OMEGA 5600 SERIES NON-INVASIVE BLOOD PRESSURE MONITORSNovember 20, 1995
K935020OMNI-TRAC MODIFICATIONApril 26, 1995
K936051OMNI-CENTRAL STATION MONITORJuly 6, 1994
K890817OMNI-TRAK (PATIENT MONITOR)August 10, 1989