Lamont Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Panbus Digital Eeg & Sleep Acquisition Devices Ref K042364
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lamont Medical, Inc. have in the registry?
The registry currently lists 2 devices for Lamont Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lamont Medical, Inc.'s devices?
Among its 2 most recently registered devices, Lamont Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Lamont Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Lamont Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lamont Medical, Inc. in the registry?
The most recently registered devices listed for Lamont Medical, Inc. include WARATAH DIGITAL EEG AND SLEEP ACQUISITION DEVICES WITH, OR WITHOUT, PULSE OXIMETRY, CARDINAL DIGITAL EEG AND SLEEP ACQUIS and PANBUS DIGITAL EEG & SLEEP ACQUISITION DEVICES.