Diagnostic Information, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Diagnostic Information, Inc. makes
Diagnostic Information, Inc. manufactures positron emission tomography (PET) imaging systems, including the PET-SCOPE II (Model DIS-1611) and standalone PET-SCOPE devices, as well as PET-TV X-ray image intensifier systems designed for hybrid diagnostic imaging.
These devices are classified as Class II under FDA regulations and are authorised through the 510(k) clearance process. The company is based in the United States.
Catalogue
Pet-Scope Ii Model Dis-1611 Ref K801166
Regimes: 510(k) Registry: 510(k)Pet-Tv X-Ray Image Intensifier System Ref K771485
Regimes: 510(k) Registry: 510(k)Pet-Scope Ref K761285
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Diagnostic Information, Inc. have in the registry?
The registry currently lists 3 devices for Diagnostic Information, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diagnostic Information, Inc.'s devices?
Among its 3 most recently registered devices, Diagnostic Information, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Diagnostic Information, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Diagnostic Information, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Diagnostic Information, Inc. in the registry?
The most recently registered devices listed for Diagnostic Information, Inc. include PET-SCOPE II MODEL DIS-1611, PET-TV X-RAY IMAGE INTENSIFIER SYSTEM and PET-SCOPE.