Laboratoires Luneau
FranceFDA applicant, unverified
- Devices
- 1
What Laboratoires Luneau makes
Laboratoires Luneau manufactures umbilical cord clamps, which are used during childbirth to secure and control the umbilical cord after delivery.
The company’s products are classified as Class II devices under FDA regulations and are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Luneau Umbilical Cord Clamp Ref K923439
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Laboratoires Luneau have in the registry?
The registry currently lists 1 device for Laboratoires Luneau. Devices recorded under merged duplicate company entries are counted once.
Which registries list Laboratoires Luneau's devices?
Among its 1 most recently registered device, Laboratoires Luneau has devices listed in FDA 510(k) (1 device).
What risk classes do Laboratoires Luneau's devices fall under?
Among its 1 most recently registered device, the classes recorded for Laboratoires Luneau's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Laboratoires Luneau in the registry?
The most recently registered devices listed for Laboratoires Luneau include LUNEAU UMBILICAL CORD CLAMP.