Medical Device Manufacturer · US , Walker , MI

Catheter Technology Corp. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1983

Total

Cleared

Denied

Catheter Technology Corp. has 13 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 13 cleared submissions from 1983 to 1988. Primary specialty: General Hospital.

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

Catheter Technology Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Catheter Technology Corp.

13 devices

1-12 of 13

Cleared Mar 04, 1988

CATH-TECH PORT IMPLANTABLE VASCULAR ACCESS SYSTEM

K880571 · LJT

General Hospital · 23d

Cleared Aug 12, 1987

PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER

K871080 · DQY

Cardiovascular · 147d

Cleared Jun 24, 1987

GROSHONG CV CATHETER REPAIR KIT

K871998 · LJS

General Hospital · 29d

Cleared Mar 28, 1986

BRAWN AND GROSHONG CATHETERS

K860256 · FOZ

General Hospital · 63d

Cleared Mar 13, 1985

CATH-TECH POLYURETHANE UMBILICAL VESS

K842577 · FOZ

General Hospital · 253d

Cleared Oct 02, 1984

CATH-TECH CHOLANGIOGRAPHY CATHETER

K842147 · FGE

Gastroenterology & Urology · 125d

Cleared Jul 25, 1984

UMBILICAL VESSEL CATHETER

K840339 · FOS

General Hospital · 182d

Cleared Oct 14, 1983

GROSHONG CATHETER, LONG TERM TYPE

K831386 · LJS

General Hospital · 169d

Catheter Technology Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Catheter Technology Corp.

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