Carapac Systems, Inc.
Country not established
- Devices
- 1
What Carapac Systems, Inc. makes
Carapac Systems, Inc. manufactures the UNI-THANE, a medical device designed for use in vascular access applications, including central venous catheters and related systems.
The UNI-THANE is classified as a Class I device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Uni-Thane Ref K831611
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Carapac Systems, Inc. have in the registry?
The registry currently lists 1 device for Carapac Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Carapac Systems, Inc.'s devices?
Among its 1 most recently registered device, Carapac Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Carapac Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Carapac Systems, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Carapac Systems, Inc. in the registry?
The most recently registered devices listed for Carapac Systems, Inc. include UNI-THANE.