Jung Products, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
Catalogue
Venes Ii Ref K811085
510(k) 510(k)Venes Custon Rx Ref K820484
510(k) 510(k)
Frequently asked questions
How many devices does Jung Products, Inc. have in the registry?
The registry currently lists 2 devices for Jung Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jung Products, Inc.'s devices?
Among its 2 most recently registered devices, Jung Products, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Jung Products, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Jung Products, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jung Products, Inc. in the registry?
The most recently registered devices listed for Jung Products, Inc. include VENES II and VENES CUSTON RX.