Clinico
GermanyFDA applicant, unverified
- Devices
- 2
What Clinico makes
Clinico makes the TAKY-SPIKE PLUS and PERFUDROP AIR M-P WITH NEEDLE 20 G, MODEL 48451606 devices.
These devices are Class II medical devices listed in the FDA 510(k) registry, and Clinico is based in the United States.
Catalogue
Taky-Spike Plus Ref K974198
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Clinico have in the registry?
The registry currently lists 2 devices for Clinico. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clinico's devices?
Among its 2 most recently registered devices, Clinico has devices listed in FDA 510(k) (2 devices).
What risk classes do Clinico's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Clinico's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clinico in the registry?
The most recently registered devices listed for Clinico include TAKY-SPIKE PLUS and PERFUDROP AIR M-P WITH NEEDLE 20 G, MODEL 48451606.