Radiation Monitoring Devices, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Modification To Gamma Guidance System Ref K983768
Regimes: 510(k) Registry: 510(k)Gamma Guidance System Ref K961321
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Radiation Monitoring Devices, Inc. have in the registry?
The registry currently lists 2 devices for Radiation Monitoring Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Radiation Monitoring Devices, Inc.'s devices?
Among its 2 most recently registered devices, Radiation Monitoring Devices, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Radiation Monitoring Devices, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Radiation Monitoring Devices, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Radiation Monitoring Devices, Inc. in the registry?
The most recently registered devices listed for Radiation Monitoring Devices, Inc. include MODIFICATION TO GAMMA GUIDANCE SYSTEM and GAMMA GUIDANCE SYSTEM.