Calliope Corp.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Catarex Vitrecutter I/A Dispos. Cut Ref K840063
Regimes: 510(k) Registry: 510(k)Catarex Diap. Extracapsular Cataract Ref K832446
Regimes: 510(k) Registry: 510(k)Catarex/Ultrasonics Kit Ref K840181
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Calliope Corp. have in the registry?
The registry currently lists 3 devices for Calliope Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Calliope Corp.'s devices?
Among its 3 most recently registered devices, Calliope Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Calliope Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Calliope Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Calliope Corp. in the registry?
The most recently registered devices listed for Calliope Corp. include CATAREX VITRECUTTER I/A DISPOS. CUT, CATAREX DIAP. EXTRACAPSULAR CATARACT and CATAREX/ULTRASONICS KIT.