Headstart, Ltd.
Country not established
- Devices
- 1
What Headstart, Ltd. makes
Headstart, Ltd. manufactures the SnugKap, a device designed for pediatric respiratory support and apnea monitoring, intended to reduce the risk of sudden infant death syndrome (SIDS).
The SnugKap 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
SnugKap Ref K193383
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Headstart, Ltd. have in the registry?
The registry currently lists 1 device for Headstart, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Headstart, Ltd.'s devices?
Among its 1 most recently registered device, Headstart, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Headstart, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Headstart, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Headstart, Ltd. in the registry?
The most recently registered devices listed for Headstart, Ltd. include SnugKap.