Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of PhilipsLabelled by claude-sonnet-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Invivo Research with 14 510(k) clearances. The most recent is a 510(k) clearance dated Aug 26, 2005: MRI COMPATIBLE PATIENT MONITORING SYSTEM, MODEL 3160.
| Aug 26, 2005 | MRI COMPATIBLE PATIENT MONITORING SYSTEM, MODEL 3160K050399 · MWI | 510(k) clearances |
| Jan 10, 2005 | MODULAR TELEMETRY SYSTEM FOR THE VISION TELEPAK, MODEL 20701K043354 · DRT | 510(k) clearances |
| Oct 15, 2004 | INTEGRATED PATIENT MONITORING SYSTEMK041918 · MWI | 510(k) clearances |
| Sep 22, 2004 | MAGNITUDE 3150M MRI PATIENT MONITOR, MODEL 3150MK040915 · MWI | 510(k) clearances |
| Feb 7, 2002 | CENTURION 2000 CENTRAL STATION ARRHYTHMIA PATIENT MONITORING SYSTEMK002604 · DSI | 510(k) clearances |
| Sep 26, 2000 | OMNI-TRAK 3150/3155A SERIES MONITOR WITH ANESTHETIC AGENT, MODEL 3155A SERIESK002030 · MWI | 510(k) clearances |
| Nov 16, 1998 | CENTURION CENTRAL STATION ARRHYTHMIA PATIENT MONITORING SYSTEMK980045 · DSI | 510(k) clearances |
| Oct 28, 1998 | MILLENNIA 3500 SERIES MONITOR WITH ANTHESTHETIC AGENTK974581 · DRT | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
