Shenzzhen Luckcome Technology Inc., Ltd.
ChinaFDA applicant, unverified
- Devices
- 1
What Shenzzhen Luckcome Technology Inc., Ltd. makes
Shenzhen Luckcome Technology Inc., Ltd. manufactures the Fetal Doppler (Model FD88), a handheld device used for non-invasive prenatal monitoring of fetal heart rate.
The Fetal Doppler (Model FD88) is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Fetal Doppler, Model FD88 Ref K182710
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Shenzzhen Luckcome Technology Inc., Ltd. have in the registry?
The registry currently lists 1 device for Shenzzhen Luckcome Technology Inc., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Shenzzhen Luckcome Technology Inc., Ltd.'s devices?
Among its 1 most recently registered device, Shenzzhen Luckcome Technology Inc., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Shenzzhen Luckcome Technology Inc., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Shenzzhen Luckcome Technology Inc., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Shenzzhen Luckcome Technology Inc., Ltd. in the registry?
The most recently registered devices listed for Shenzzhen Luckcome Technology Inc., Ltd. include Fetal Doppler, Model FD88.