Jamjoom Fullcare Corporation
ChinaFDA applicant, unverified
- Devices
- 1
What Jamjoom Fullcare Corporation makes
Jamjoom Fullcare Corporation manufactures sterile, pre-packaged Nelaton catheters, designed for single-use medical procedures such as drainage or fluid administration.
These devices are classified as Class II under US regulations and are listed via the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Ready to use Nelaton Catheter Ref K251178
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jamjoom Fullcare Corporation have in the registry?
The registry currently lists 1 device for Jamjoom Fullcare Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jamjoom Fullcare Corporation's devices?
Among its 1 most recently registered device, Jamjoom Fullcare Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Jamjoom Fullcare Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Jamjoom Fullcare Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jamjoom Fullcare Corporation in the registry?
The most recently registered devices listed for Jamjoom Fullcare Corporation include Ready to use Nelaton Catheter.