Cape Tech Medical Products
Country not established
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Guide-Tech Encapsulated Guidewire Ref K926039
Regimes: 510(k) Registry: 510(k)Heli-Tech Retrieval Basket Ref K926040
Regimes: 510(k) Registry: 510(k)Flex-Tech Balloon Dilator Ref K926038
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cape Tech Medical Products have in the registry?
The registry currently lists 3 devices for Cape Tech Medical Products. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cape Tech Medical Products's devices?
Among its 3 most recently registered devices, Cape Tech Medical Products has devices listed in FDA 510(k) (3 devices).
What risk classes do Cape Tech Medical Products's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Cape Tech Medical Products's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cape Tech Medical Products in the registry?
The most recently registered devices listed for Cape Tech Medical Products include GUIDE-TECH ENCAPSULATED GUIDEWIRE, HELI-TECH RETRIEVAL BASKET and FLEX-TECH BALLOON DILATOR.