Medical Device Manufacturer · US , Costa Mesa , CA

American Omni Medical, Inc. - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 1985

Total

Cleared

Denied

American Omni Medical, Inc. has 20 FDA 510(k) cleared cardiovascular devices. Based in Costa Mesa, US.

Historical record: 20 cleared submissions from 1985 to 1993.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by American Omni Medical, Inc.

20 devices

1-12 of 20

Cleared Mar 08, 1993

FLOW CONROL VALVE

K922781 · MJJ

Cardiovascular · 272d

Cleared Feb 12, 1993

FLOW CONTROL VALVE, CAT. NO. ACV-38

K922356 · MJJ

Cardiovascular · 269d

Cleared Apr 03, 1990

PREBYPASS FILTER, CAT. NO. FPB-5

K900672 · KRJ

Cardiovascular · 49d

Cleared Jan 30, 1989

CARDIOTOMY RESERVOIR VALVE NO. CRV-30 OR PCRV-25

K884893 · KRI

Cardiovascular · 69d

Cleared Jan 24, 1989

CARDIOPLEGIA OVERPRESSURE VALVE CPOP-350 & 700

K884640 · KRI

Cardiovascular · 78d

Cleared Jul 14, 1988

BUBBLE TRAP-FILTER CAT. NO B180F37

K873316 · DTM

Cardiovascular · 330d

Cleared Feb 29, 1988

AIR VENT LINE CAT. NO. AVL-36

K875080 · DTM

Cardiovascular · 82d

Cleared Nov 06, 1987

PRESSURE BARRIER KIT CAT. NO. PBK-3

K873802 · DXS

Cardiovascular · 49d

Cleared Nov 05, 1987

PEDIATRIC BUBBLE TRAP CAT. NO. B-100

K873610 · BSY

Anesthesiology · 58d

Cleared Oct 07, 1987

SILENT GUARD CAT. NO. SG-10

K873488 · DTL

Cardiovascular · 37d

Cleared Sep 16, 1987

NASOGASTRIC VOICETUBE

K871632 · BTR

Anesthesiology · 142d

Cleared Jun 08, 1987

BUBBLE TRAP CAT. NO. B-180

K870819 · DWF

Cardiovascular · 97d

American Omni Medical, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by American Omni Medical, Inc.

Filters