Huntleigh Group, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Huntleigh Group, Ltd. makes
Huntleigh Group, Ltd. manufactures fetal monitoring devices, including the Model 2100 Fetal Monitor, which is designed for real-time assessment of fetal heart rate and uterine contractions during pregnancy.
The company’s products are regulated under the FDA’s 510(k) clearance process in the United States. The Model 2100 Fetal Monitor is listed in the FDA’s 510(k) database as a Class II medical device, adhering to regulatory standards for obstetric monitoring equipment.
Catalogue
Model 2100 Fetal Monitor Ref K837102
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Huntleigh Group, Ltd. have in the registry?
The registry currently lists 1 device for Huntleigh Group, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Huntleigh Group, Ltd.'s devices?
Among its 1 most recently registered device, Huntleigh Group, Ltd. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Huntleigh Group, Ltd. in the registry?
The most recently registered devices listed for Huntleigh Group, Ltd. include MODEL 2100 FETAL MONITOR.