Lederle Laboratories
Country not established
- Devices
- 3
What Lederle Laboratories makes
Lederle Laboratories makes a rotator with fixed speed, an anti-convulsant drug control device, and a micro/pettor SMI device.
These devices are classified as Class I and Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Rotator, Fixed Speed Ref K760467
Regimes: 510(k) Registry: 510(k)Anti-Convulsant Drug Control Ref K770975
Regimes: 510(k) Registry: 510(k)Micro/Pettor, Smi Ref K770307
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lederle Laboratories have in the registry?
The registry currently lists 3 devices for Lederle Laboratories. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lederle Laboratories's devices?
Among its 3 most recently registered devices, Lederle Laboratories has devices listed in FDA 510(k) (3 devices).
What risk classes do Lederle Laboratories's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Lederle Laboratories's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lederle Laboratories in the registry?
The most recently registered devices listed for Lederle Laboratories include ROTATOR, FIXED SPEED, ANTI-CONVULSANT DRUG CONTROL and MICRO/PETTOR, SMI.