Oximetrix, Inc.
Oximetrix, Inc. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 1986.
Top product codes for Oximetrix, Inc.
Recent clearances by Oximetrix, Inc.
- K853018 — MODEL 3000 OPTICATH COMPUTER
- K842622 — HEMO STATIC/ESU SCALPEL SYSTEM
- K833966 — PUMP INFUSION WEARABLE INFUSION PUMP
- K823007 — OPTICATH HEPARIN COATED, FLOW-DIRECT
- K821056 — FLOW DIRECTED THERMAL-DILUTION CATHETER
- K821057 — FLOW DIRECTED THERMAL-DILUTION INFUSION
- K820674 — OPTICATH
- K811391 — OXIMETRIX ACCU SAT CPB
- K791868 — OXIMETRIX SHAW HEMOSTATIC SURG. SYS.
- K781879 — HEATER, OXIMETER SYSTEM
- K781134 — CATHETER, THERMAL DILUTION FIBEROPTIC
- K760234 — OXIMETER, IN VIVO CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.