Medical Device Manufacturer · US , Mchenry , IL

Oximetrix, Inc. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1976

Total

Cleared

Denied

Oximetrix, Inc. has 12 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 12 cleared submissions from 1976 to 1986. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Oximetrix, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Oximetrix, Inc.

12 devices

1-12 of 12

Cleared Jan 13, 1986

MODEL 3000 OPTICATH COMPUTER

K853018 · DXG

Cardiovascular · 180d

Cleared Oct 23, 1984

HEMO STATIC/ESU SCALPEL SYSTEM

K842622 · GEI

General & Plastic Surgery · 110d

Cleared Jan 25, 1984

PUMP INFUSION WEARABLE INFUSION PUMP

K833966 · JSJ

Microbiology · 70d

Cleared Nov 01, 1982

OPTICATH HEPARIN COATED, FLOW-DIRECT

K823007 · DYG

Cardiovascular · 20d

Cleared May 18, 1982

FLOW DIRECTED THERMAL-DILUTION CATHETER

K821056

Cardiovascular · 33d

Cleared May 18, 1982

FLOW DIRECTED THERMAL-DILUTION INFUSION

OXIMETRIX ACCU SAT CPB

K811391 · DRY

Cardiovascular · 63d

Cleared Jan 04, 1980

OXIMETRIX SHAW HEMOSTATIC SURG. SYS.

K791868 · GEI

General & Plastic Surgery · 106d

Cleared Jan 08, 1979

HEATER, OXIMETER SYSTEM

K781879 · DQA

Anesthesiology · 63d

Cleared Aug 17, 1978

CATHETER, THERMAL DILUTION FIBEROPTIC

K781134 · DQE

Cardiovascular · 42d

Cleared Aug 23, 1976

OXIMETER, IN VIVO CATHETER

K760234 · DQE

Cardiovascular · 39d

Oximetrix, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Oximetrix, Inc.

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