Medical Device Manufacturer · US , Mchenry , IL

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

22 submissions · 18 cleared · Since 1979

Total

Cleared

Denied

Carbomedics, Inc. has 18 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 18 cleared submissions from 1979 to 1997. Primary specialty: Cardiovascular.

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

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

22 devices

1-12 of 22

Cleared Jul 25, 1997

ANNULOFLO SYSTEM

K970375 · KRH

Cardiovascular · 172d

Cleared Feb 19, 1997

VASCUTEK GELWEAVE VASCULAR GRAFT (BIFURCATED CONFIGURATION)

CARBOMEDICS MITRAL ROTATOR

K960923 · MOP

Cardiovascular · 54d

Cleared Apr 25, 1996

VASCUTEK VASCUSOFT PLUS VASCULAR GRAFT

K960706 · DSY

Cardiovascular · 64d

Cleared Apr 15, 1996

CARBOMEDICS VALVE TESTER

K960169 · DTJ

Cardiovascular · 90d

Cleared Mar 07, 1996

VASCUTEK GRAFT SIZER SET

K955588 · DSY

Cardiovascular · 91d

Cleared Nov 29, 1995

CARBOMEDICS SUPRA-ANNULAR VALVE SIZER

K952184 · DTI

Cardiovascular · 204d

Cleared Jun 20, 1995

CARBOMEDICS EXENDED MITRAL ROTATOR

K951368 · MOP

Cardiovascular · 85d

Cleared Jul 06, 1994

CARBOMEDICS(R) PROSTHETIC HEART VALVE HOLDER HANDLE

DORR HIP PROSTHESIS, ACETABULAR COMPON

K842893 · JDL

Orthopedic · 108d

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

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