New Product Development, Inc.
Country not established
- Devices
- 1
What New Product Development, Inc. makes
New Product Development, Inc. manufactures the EIDOS 5003 Holter System, a portable cardiac monitoring device designed for continuous ECG recording over extended periods to diagnose arrhythmias and other heart conditions.
The EIDOS 5003 Holter System 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
Eidos 5003 Holter System Ref K952969
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does New Product Development, Inc. have in the registry?
The registry currently lists 1 device for New Product Development, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list New Product Development, Inc.'s devices?
Among its 1 most recently registered device, New Product Development, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do New Product Development, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for New Product Development, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from New Product Development, Inc. in the registry?
The most recently registered devices listed for New Product Development, Inc. include EIDOS 5003 HOLTER SYSTEM.