Ram Development
IsraelFDA applicant, unverified
- Devices
- 2
What Ram Development makes
Ram Development manufactures stopcock valves and intrauterine catheters, designed for medical procedures requiring precise fluid control or uterine access.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Stopcock Ref K862691
Regimes: 510(k) Registry: 510(k)Intrauterine Catheter Ref K861305
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ram Development have in the registry?
The registry currently lists 2 devices for Ram Development. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ram Development's devices?
Among its 2 most recently registered devices, Ram Development has devices listed in FDA 510(k) (2 devices).
What risk classes do Ram Development's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ram Development's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ram Development in the registry?
The most recently registered devices listed for Ram Development include STOPCOCK and INTRAUTERINE CATHETER.