Digital Cardiovascular Instruments, Inc.
Country not established
- Devices
- 1
What Digital Cardiovascular Instruments, Inc. makes
Digital Cardiovascular Instruments, Inc. manufactures the DCI Model EP-2 Clinical Stimulator, a device designed for electrophysiological studies and catheter ablation procedures in cardiac electrophysiology.
The company’s portfolio is regulated under FDA Class II devices, with the DCI Model EP-2 Clinical Stimulator authorised via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Dci Model Ep-2 Clinical Stimulator Ref K854196
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Digital Cardiovascular Instruments, Inc. have in the registry?
The registry currently lists 1 device for Digital Cardiovascular Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Digital Cardiovascular Instruments, Inc.'s devices?
Among its 1 most recently registered device, Digital Cardiovascular Instruments, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Digital Cardiovascular Instruments, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Digital Cardiovascular Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Digital Cardiovascular Instruments, Inc. in the registry?
The most recently registered devices listed for Digital Cardiovascular Instruments, Inc. include DCI MODEL EP-2 CLINICAL STIMULATOR.