Cardiocom, LLC
United StatesFDA applicant, unverified
- Devices
- 5
What Cardiocom, LLC makes
Cardiocom, LLC manufactures non-invasive blood pressure monitoring systems, including standalone devices like the Commander III and integrated tablet solutions for clinical and home use. These systems measure and record blood pressure readings, with some models designed for ambulatory or continuous monitoring in controlled environments.
The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The portfolio is regulated in the United States, where the manufacturer is based.
Catalogue
Cardiocom Commander Iii Ref K053303
Regimes: 510(k) Registry: 510(k)Commander Iii Non-Invasive Blood Pressure System Ref K053304
Regimes: 510(k) Registry: 510(k)Tablet Commander Ref K122285
Regimes: 510(k) Registry: 510(k)Commander Ii Ref K043096
Regimes: 510(k) Registry: 510(k)Commander 111, Model CD300-CD399 Ref K091821
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardiocom, LLC have in the registry?
The registry currently lists 5 devices for Cardiocom, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardiocom, LLC's devices?
Among its 5 most recently registered devices, Cardiocom, LLC has devices listed in FDA 510(k) (5 devices).
What risk classes do Cardiocom, LLC's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Cardiocom, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardiocom, LLC in the registry?
The most recently registered devices listed for Cardiocom, LLC include CARDIOCOM COMMANDER III, COMMANDER III NON-INVASIVE BLOOD PRESSURE SYSTEM, TABLET COMMANDER and COMMANDER II.