Cardio Design Pty., Ltd.
Country not established
- Devices
- 2
What Cardio Design Pty., Ltd. makes
Cardio Design Pty. Ltd. manufactures perineometer devices, including the Peritron Perineometer (Model 9300V or 9300A) and the Peritron, which are used to measure perineal muscle function and pelvic floor strength.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Peritron Perineometer Model 9300V Or 9300A Ref K983052
Regimes: 510(k) Registry: 510(k)Peritron Ref K945611
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardio Design Pty., Ltd. have in the registry?
The registry currently lists 2 devices for Cardio Design Pty., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardio Design Pty., Ltd.'s devices?
Among its 2 most recently registered devices, Cardio Design Pty., Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Cardio Design Pty., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cardio Design Pty., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardio Design Pty., Ltd. in the registry?
The most recently registered devices listed for Cardio Design Pty., Ltd. include PERITRON PERINEOMETER MODEL 9300V OR 9300A and PERITRON.