Catheter Technology Corp.
FDA 510(k) medical device clearances.
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.