Medical Device Manufacturer · US , Mchenry , IL

Medi-Tech, Inc. - FDA 510(k) Cleared Devices

36 submissions · 35 cleared · Since 1978

36

Total

35

Cleared

0

Denied

FDA 510(k) Regulatory Record - Medi-Tech, Inc. Cardiovascular ✕

13 devices

1-12 of 13

Cleared May 15, 1996

MEDI-TECH EDDY INTRAVASCULAR INFUSION CATHETER

Cardiovascular · 233d

Cleared Aug 17, 1995

MEDI-TECH PLATFORM GUIDE CATHETER

Cardiovascular · 90d

Cleared Apr 21, 1989

IMAGER FLUSH CATHETERS

Cardiovascular · 186d

Cleared Apr 06, 1989

KATZEN THROMBOLYSIS GUIDEWIRE

Cardiovascular · 205d

Cleared Nov 04, 1988

TITANIUM GREENFIELD VENA CAVA FILTER CARRIER

Cardiovascular · 393d

Cleared Apr 22, 1988

PERIPHERAL DILATATION CATHETER

Cardiovascular · 88d

Cleared Apr 09, 1987

MEDI-TECH SELECTIVE TORQUE CATHETER

Cardiovascular · 170d

Cleared Apr 09, 1987

TITANIUM PERCUTANEOUS GREENFIELD VENA CAVE FILTER

Cardiovascular · 43d

Cleared Nov 01, 1985

PERCUTANEOUS GREENFIELD VENA CAVA FILTER SYSTEM

Cardiovascular · 170d

Cleared Jun 10, 1985

LEVEEN INFLATOR DISPOSABLE INFLATION SYRINGE

Cardiovascular · 62d

Cleared Nov 29, 1984

WIREGUIDE OR GUIDEWIRE

Cardiovascular · 121d

Cleared Oct 24, 1984

MEDI-TECH DILATATION CATHETERS

Cardiovascular · 57d