Litton Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Pulse Klystron Amplifier (L-5822-00) Ref K951142
Regimes: 510(k) Registry: 510(k)Pulse Klystron Amplififer (L-5822-90) Ref K951143
Regimes: 510(k) Registry: 510(k)Oxygen/Sterile Air Gen Syst/Surgical Handpieces Ref K873284
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Litton Systems, Inc. have in the registry?
The registry currently lists 4 devices for Litton Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Litton Systems, Inc.'s devices?
Among its 4 most recently registered devices, Litton Systems, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Litton Systems, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Litton Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Litton Systems, Inc. in the registry?
The most recently registered devices listed for Litton Systems, Inc. include PATIENT VENTILATION OXYGEN CONCENTRATING SYSTEM (PVOCS), PULSE KLYSTRON AMPLIFIER (L-5822-00), PULSE KLYSTRON AMPLIFIFER (L-5822-90) and OXYGEN/STERILE AIR GEN SYST/SURGICAL HANDPIECES.