Catheter Technology Corp.
Catheter Technology Corp. holds FDA 510(k) medical device clearances, first cleared 1983, most recent 1988.
Top product codes for Catheter Technology Corp.
Recent clearances by Catheter Technology Corp.
- K880571 — CATH-TECH PORT IMPLANTABLE VASCULAR ACCESS SYSTEM
- K871080 — PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER
- K871998 — GROSHONG CV CATHETER REPAIR KIT
- K860256 — BRAWN AND GROSHONG CATHETERS
- K842577 — CATH-TECH POLYURETHANE UMBILICAL VESS
- K842147 — CATH-TECH CHOLANGIOGRAPHY CATHETER
- K840339 — UMBILICAL VESSEL CATHETER
- K831386 — GROSHONG CATHETER, LONG TERM TYPE
- K831361 — BETA-PREG
- K831365 — TESTCORP ANA
- K831366 — TESTCORP PREG
- K831362 — TESTCORP CRP
- K831363 — TESTCORP ASO
Data sourced from openFDA. This site is unofficial and independent of the FDA.