Taris Corp.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Thieler Kit Ref K875153
Regimes: 510(k) Registry: 510(k)Non Coring Infusion Set Ref K881256
Regimes: 510(k) Registry: 510(k)Neocath Ref K880887
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Taris Corp. have in the registry?
The registry currently lists 3 devices for Taris Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Taris Corp.'s devices?
Among its 3 most recently registered devices, Taris Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Taris Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Taris Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Taris Corp. in the registry?
The most recently registered devices listed for Taris Corp. include THIELER KIT, NON CORING INFUSION SET and NEOCATH.