Perimeter Medical Imaging, Inc.
CanadaFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
OTIS Optical Coherence Tomography SYstem Ref K190404
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
OTIS Optical Coherence Tomography System Ref K171560
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Perimeter Medical Imaging, Inc. have in the registry?
The registry currently lists 3 devices for Perimeter Medical Imaging, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Perimeter Medical Imaging, Inc.'s devices?
Among its 3 most recently registered devices, Perimeter Medical Imaging, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Perimeter Medical Imaging, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Perimeter Medical Imaging, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Perimeter Medical Imaging, Inc. in the registry?
The most recently registered devices listed for Perimeter Medical Imaging, Inc. include OTIS Optical Coherence Tomography SYstem and Perimeter Otis™ 1.0 Optical Coherence Tomography System.