Clinical Data Instruments, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Clinical Data Instruments, Inc. makes
Clinical Data Instruments, Inc. manufactures neonatal flotation systems for respiratory support in infants, including the NEO-FLOAT system, as well as cardiac detection devices like the CENTURION. The company also produces ambulatory pH recording devices for monitoring gastrointestinal function.
These devices are regulated under FDA 510(k) clearance, with products classified as Class I and Class II. The company is based in the United States.
Catalogue
Neo-Float Neonatal Flotation Sys & Rhyt Ref K832829
Regimes: 510(k) Registry: 510(k)Centurion Cardiac Detector Ref K832828
Regimes: 510(k) Registry: 510(k)Ambulatory Ph Recording Device Ref K842349
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Clinical Data Instruments, Inc. have in the registry?
The registry currently lists 3 devices for Clinical Data Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clinical Data Instruments, Inc.'s devices?
Among its 3 most recently registered devices, Clinical Data Instruments, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Clinical Data Instruments, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Clinical Data Instruments, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clinical Data Instruments, Inc. in the registry?
The most recently registered devices listed for Clinical Data Instruments, Inc. include NEO-FLOAT NEONATAL FLOTATION SYS & RHYT, CENTURION CARDIAC DETECTOR and AMBULATORY PH RECORDING DEVICE.