Sensidyne, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Sensaid Ref K011974
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sensidyne, Inc. have in the registry?
The registry currently lists 4 devices for Sensidyne, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sensidyne, Inc.'s devices?
Among its 4 most recently registered devices, Sensidyne, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Sensidyne, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Sensidyne, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sensidyne, Inc. in the registry?
The most recently registered devices listed for Sensidyne, Inc. include 100 SERIES OXYGEN ANALYZER, MODELS 1000-E AND 1000-I, SENSAID, SENSIDYNE OXYGEN ANALYZER & SENSIDYNE OXYGEN MONITOR and SENSAID, MODELS# RC-NVA30-10; RC-CS140-10; RC-BC150-3.