Covidien LP, Formerly Registered AS Kendall
United StatesFDA applicant, unverified
- Devices
- 3
What Covidien LP, Formerly Registered AS Kendall makes
Covidien manufactures vascular access devices, including hemodialysis catheters like the Palindrome P, and enteral feeding tubes such as the Dobhoff dual-port tube. Their portfolio also includes umbilical vessel catheters, such as the modified Argyle polyurethane catheters in 2.5FR, 3.5FR, and 5FR sizes.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Palindrome P Hemodialysis Catheter Ref K092205
Regimes: 510(k) Registry: 510(k)Dobbhoff Dual Port Feeding Tube Ref K112511
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Covidien Lp, Formerly Registered AS Kendall have in the registry?
The registry currently lists 3 devices for Covidien Lp, Formerly Registered AS Kendall. Devices recorded under merged duplicate company entries are counted once.
Which registries list Covidien Lp, Formerly Registered AS Kendall's devices?
Among its 3 most recently registered devices, Covidien Lp, Formerly Registered AS Kendall has devices listed in FDA 510(k) (3 devices).
What risk classes do Covidien Lp, Formerly Registered AS Kendall's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Covidien Lp, Formerly Registered AS Kendall's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Covidien Lp, Formerly Registered AS Kendall in the registry?
The most recently registered devices listed for Covidien Lp, Formerly Registered AS Kendall include PALINDROME P HEMODIALYSIS CATHETER, DOBBHOFF DUAL PORT FEEDING TUBE and MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR..