Invivo Research, Inc.
FDA 510(k) medical device clearances.
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.