Mcdonnell Douglas Corp.
Country not established
- Devices
- 1
What Mcdonnell Douglas Corp. makes
McDonnell Douglas Corp. manufactures an anticonvulsant control serum, designed for managing seizures in clinical settings.
The anticonvulsant control serum is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Anticonvulsant Control Serum Ref K780142
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mcdonnell Douglas Corp. have in the registry?
The registry currently lists 1 device for Mcdonnell Douglas Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mcdonnell Douglas Corp.'s devices?
Among its 1 most recently registered device, Mcdonnell Douglas Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Mcdonnell Douglas Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mcdonnell Douglas Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Mcdonnell Douglas Corp. in the registry?
The most recently registered devices listed for Mcdonnell Douglas Corp. include ANTICONVULSANT CONTROL SERUM.