Invivo Research, Inc.
Invivo Research, Inc. holds FDA 510(k) medical device clearances, first cleared 1989, most recent 2005.
Top product codes for Invivo Research, Inc.
Recent clearances by Invivo Research, Inc.
- K050399 — MRI COMPATIBLE PATIENT MONITORING SYSTEM, MODEL 3160
- K043354 — MODULAR TELEMETRY SYSTEM FOR THE VISION TELEPAK, MODEL 20701
- K041918 — INTEGRATED PATIENT MONITORING SYSTEM
- K040915 — MAGNITUDE 3150M MRI PATIENT MONITOR, MODEL 3150M
- K002604 — CENTURION 2000 CENTRAL STATION ARRHYTHMIA PATIENT MONITORING SYSTEM
- K002030 — OMNI-TRAK 3150/3155A SERIES MONITOR WITH ANESTHETIC AGENT, MODEL 3155A SERIES
- K980045 — CENTURION CENTRAL STATION ARRHYTHMIA PATIENT MONITORING SYSTEM
- K974581 — MILLENNIA 3500 SERIES MONITOR WITH ANTHESTHETIC AGENT
- K971840 — OMNI-TRAK MODEL 3150 SERIES PATIENT MONITORING SYSTEM
- K955045 — OMNI-TRAK PATIENT MONITORING SYSTEM
- K945138 — OMEGA 5600 SERIES NON-INVASIVE BLOOD PRESSURE MONITORS
- K935020 — OMNI-TRAC MODIFICATION
- K936051 — OMNI-CENTRAL STATION MONITOR
- K890817 — OMNI-TRAK (PATIENT MONITOR)
Data sourced from openFDA. This site is unofficial and independent of the FDA.