Chronodynamics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Chronodynamics, Inc. makes
Chronodynamics, Inc. manufactures the Chronodynamics Data Recorder (CDR)-100, a device designed for capturing and storing physiological or performance data, likely for clinical or research use.
The CDR-100 is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Hemo-Pulse 2000 Ref K914142
Regimes: 510(k) Registry: 510(k)Chronodynamics Data Recorder (Cdr)-100 Ref K881813
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Chronodynamics, Inc. have in the registry?
The registry currently lists 2 devices for Chronodynamics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Chronodynamics, Inc.'s devices?
Among its 2 most recently registered devices, Chronodynamics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Chronodynamics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Chronodynamics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Chronodynamics, Inc. in the registry?
The most recently registered devices listed for Chronodynamics, Inc. include HEMO-PULSE 2000 and CHRONODYNAMICS DATA RECORDER (CDR)-100.