Cardio-Dynamics Laboratories, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ecg Electrode, 2021, 2022, 2032, 2033 Ref K781514
Regimes: 510(k) Registry: 510(k)Foam Ecg Electrode, 2060 And 2061 Ref K770988
Regimes: 510(k) Registry: 510(k)Ecg Analyzer, High Speed Ref K781911
Regimes: 510(k) Registry: 510(k)Electrocardiographic Ecg Recorder Ref K781152
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardio-Dynamics Laboratories, Inc. have in the registry?
The registry currently lists 4 devices for Cardio-Dynamics Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardio-Dynamics Laboratories, Inc.'s devices?
Among its 4 most recently registered devices, Cardio-Dynamics Laboratories, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Cardio-Dynamics Laboratories, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Cardio-Dynamics Laboratories, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardio-Dynamics Laboratories, Inc. in the registry?
The most recently registered devices listed for Cardio-Dynamics Laboratories, Inc. include ECG ELECTRODE, 2021, 2022, 2032, 2033, FOAM ECG ELECTRODE, 2060 AND 2061, ECG ANALYZER, HIGH SPEED and ELECTROCARDIOGRAPHIC ECG RECORDER.