Corpak Medsystems
Corpak Medsystems holds FDA 510(k) medical device clearances, first cleared 1982, most recent 2014.
Top product codes for Corpak Medsystems
Recent clearances by Corpak Medsystems
- K142012 — FARRELL VALVE SYSTEM WITH EQUILIBRIUM TECHNOLOGY AND ENFIT ENTERAL CONNECTORS
- K133599 — CORGRIP
- K131532 — ELECTROMAGNETIC TRANSMITTING STYLET
- K113351 — CORTRAK ENTERAL ACCESS DEVICE
- K100365 — FARRELL VALVE WITH CORFLO ANTI-IV CONNECTORS MODEL 20-4300AIV
- K091637 — CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900
- K083776 — CORFLO ANTI IV ENTERAL FEEDING SET, MODEL: 20-1030AIV-LB-S
- K083791 — CORFLO ANTI IV ENTERAL FEEDING SET, MODEL: 20-1060AIV-S
- K083786 — CORFLO ANTI-IV ENTERAL FEEDING EXTENSION SET, MODELS 20-1006AIV-LB AND 20-1030AIV-LB
- K083121 — NEO MAPCATH SENSOR STYLET
- K083210 — CORFLO ANTI IV ENTERAL FEEDING TUBE
- K990127 — CORFLO CUBBY LOW PROFILE GASTROSTOMY DEVICE (LPGD)
- K840656 — ENTERNAL Y EXTENSION SET RECORDER
- K831328 — NEONATAL NASOGASTRIC FEEDING TUBE-
- K821906 — CORPAK ENTERIC FEEDING TUBE W/GUIDE TIP
Data sourced from openFDA. This site is unofficial and independent of the FDA.