Cardiodyne General, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Cardiodyne General, Inc. makes
Cardiodyne General, Inc. manufactures blood pressure monitoring devices, including the Sphygmolog II Model D and the Sphygmolog, which are designed for clinical measurement of systolic and diastolic blood pressure.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Sphygmolog Ii Model D Ref K830184
Regimes: 510(k) Registry: 510(k)Syphgmolog Ref K811079
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardiodyne General, Inc. have in the registry?
The registry currently lists 2 devices for Cardiodyne General, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardiodyne General, Inc.'s devices?
Among its 2 most recently registered devices, Cardiodyne General, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Cardiodyne General, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cardiodyne General, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardiodyne General, Inc. in the registry?
The most recently registered devices listed for Cardiodyne General, Inc. include SPHYGMOLOG II MODEL D and SYPHGMOLOG.