Pt&E
Country not established
- Devices
- 1
What Pt&E makes
Pt&E manufactures an electronic Apgar timer, a device used in neonatal care to measure and display the Apgar score for newborns at 1 and 5 minutes after birth.
The electronic Apgar timer is classified as a Class I medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Electronic Apgar Timer Ref K811424
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pt&E have in the registry?
The registry currently lists 1 device for Pt&E. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pt&E's devices?
Among its 1 most recently registered device, Pt&E has devices listed in FDA 510(k) (1 device).
What risk classes do Pt&E's devices fall under?
Among its 1 most recently registered device, the classes recorded for Pt&E's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Pt&E in the registry?
The most recently registered devices listed for Pt&E include ELECTRONIC APGAR TIMER.