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Invivo Research, Inc.

14 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
MRI COMPATIBLE PATIENT MONITORING SYSTEM, MODEL 3160 (K050399)Invivo Research, Inc.2005-08-26
MODULAR TELEMETRY SYSTEM FOR THE VISION TELEPAK, MODEL 20701 (K043354)Invivo Research, Inc.2005-01-10
INTEGRATED PATIENT MONITORING SYSTEM (K041918)Invivo Research, Inc.2004-10-15
MAGNITUDE 3150M MRI PATIENT MONITOR, MODEL 3150M (K040915)Invivo Research, Inc.2004-09-22
CENTURION 2000 CENTRAL STATION ARRHYTHMIA PATIENT MONITORING SYSTEM (K002604)Invivo Research, Inc.2002-02-07
OMNI-TRAK 3150/3155A SERIES MONITOR WITH ANESTHETIC AGENT, MODEL 3155A SERIES (K002030)Invivo Research, Inc.2000-09-26
CENTURION CENTRAL STATION ARRHYTHMIA PATIENT MONITORING SYSTEM (K980045)Invivo Research, Inc.1998-11-16
MILLENNIA 3500 SERIES MONITOR WITH ANTHESTHETIC AGENT (K974581)Invivo Research, Inc.1998-10-28
OMNI-TRAK MODEL 3150 SERIES PATIENT MONITORING SYSTEM (K971840)Invivo Research, Inc.1998-03-04
OMNI-TRAK PATIENT MONITORING SYSTEM (K955045)Invivo Research, Inc.1996-07-11
OMEGA 5600 SERIES NON-INVASIVE BLOOD PRESSURE MONITORS (K945138)Invivo Research, Inc.1995-11-20
OMNI-TRAC MODIFICATION (K935020)Invivo Research, Inc.1995-04-26
OMNI-CENTRAL STATION MONITOR (K936051)Invivo Research, Inc.1994-07-06
OMNI-TRAK (PATIENT MONITOR) (K890817)Invivo Research, Inc.1989-08-10

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Every clearance here is in the API, with alerts when new ones post.