Invivo Research, Inc. is one of 20536 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Invivo Research, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MRI COMPATIBLE PATIENT MONITORING SYSTEM, MODEL 3160, MODULAR TELEMETRY SYSTEM FOR THE VISION TELEPAK, MODEL 20701, INTEGRATED PATIENT MONITORING SYSTEM
14
Total
14
Cleared
0
Denied
Invivo Research, Inc. has 14 FDA 510(k) cleared cardiovascular devices. Based in Orlando, US.
Historical record: 14 cleared submissions from 1989 to 2005.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Invivo Research, Inc.
14 devices
Cleared
Aug 26, 2005
MRI COMPATIBLE PATIENT MONITORING SYSTEM, MODEL 3160
Cardiovascular
191d
Cleared
Jan 10, 2005
MODULAR TELEMETRY SYSTEM FOR THE VISION TELEPAK, MODEL 20701
Cardiovascular
35d
Cleared
Oct 15, 2004
INTEGRATED PATIENT MONITORING SYSTEM
Cardiovascular
91d
Cleared
Sep 22, 2004
MAGNITUDE 3150M MRI PATIENT MONITOR, MODEL 3150M
Cardiovascular
167d
Cleared
Feb 07, 2002
CENTURION 2000 CENTRAL STATION ARRHYTHMIA PATIENT MONITORING SYSTEM
Cardiovascular
534d
Cleared
Sep 26, 2000
OMNI-TRAK 3150/3155A SERIES MONITOR WITH ANESTHETIC AGENT, MODEL 3155A SERIES
Cardiovascular
85d
Cleared
Nov 16, 1998
CENTURION CENTRAL STATION ARRHYTHMIA PATIENT MONITORING SYSTEM
Cardiovascular
314d
Cleared
Oct 28, 1998
MILLENNIA 3500 SERIES MONITOR WITH ANTHESTHETIC AGENT
Cardiovascular
324d
Cleared
Mar 04, 1998
OMNI-TRAK MODEL 3150 SERIES PATIENT MONITORING SYSTEM
Cardiovascular
289d
Cleared
Jul 11, 1996
OMNI-TRAK PATIENT MONITORING SYSTEM
Cardiovascular
251d
Cleared
Nov 20, 1995
OMEGA 5600 SERIES NON-INVASIVE BLOOD PRESSURE MONITORS
Cardiovascular
396d
Cleared
Apr 26, 1995
OMNI-TRAC MODIFICATION
Cardiovascular
553d