Medical Device Manufacturer · US , Mchenry , IL

Omnicon Medical Corp. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1976

Total

Cleared

Denied

Omnicon Medical Corp. has 10 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 10 cleared submissions from 1976 to 1983. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Omnicon Medical Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Omnicon Medical Corp.

10 devices

1-10 of 10

Cleared Jan 21, 1983

EMERGENCY TRACHEOSTOMY KIT

K823872 · EWC

Ear, Nose, Throat · 25d

Cleared Mar 18, 1982

MAINFLOW BACTERIA FILTER

K820576 · CAH

General Hospital · 15d

Cleared Mar 18, 1982

ANESTHESIA BACTERIA FILTER

K820577 · CAH

General Hospital · 15d

Cleared Aug 13, 1980

MAINFLOW BACTERIA FILTER

K801803 · CAH

General Hospital · 15d

Cleared Aug 13, 1980

ANESTHESIA BACTERIA FILTER

K801804 · CAH

General Hospital · 15d

Cleared Dec 20, 1977

PROTECT IV GARD

K772060 · FMP

General Hospital · 50d

Cleared Feb 14, 1977

DISPOSABLE BACTERIA FILTER

K770136 · CAH

General Hospital · 21d

Cleared Jan 12, 1977

AIRWAY, BERMAN 40, 60, 80, 90, L00MM'S

K770001 · CAE

Anesthesiology · 9d

Cleared Oct 27, 1976

CONDUCTIVE ANESTHESIA BREATHING CIRCUIT

K760819 · CAI

Anesthesiology · 15d

Cleared Jul 19, 1976

CONDUCTIVE ANESTHSIA BREATH. CIRCUIT

K760149 · CAI

Anesthesiology · 19d

Omnicon Medical Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Omnicon Medical Corp.

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