Advanced Diagnostics, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Advanced Diagnostics, Inc. makes
Advanced Diagnostics, Inc. manufactures diagnostic imaging systems, including the AVERA and ALTAIR models for diffractive energy imaging, the OS-2000 optical sonography system, and a mid-stream pregnancy test strip.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Mid Stream Pregnancy Test Ref K023037
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Os-2000 Optical Sonography System Ref K001510
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Advanced Diagnostics, Inc. have in the registry?
The registry currently lists 4 devices for Advanced Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Advanced Diagnostics, Inc.'s devices?
Among its 4 most recently registered devices, Advanced Diagnostics, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Advanced Diagnostics, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Advanced Diagnostics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Advanced Diagnostics, Inc. in the registry?
The most recently registered devices listed for Advanced Diagnostics, Inc. include AVERA MODEL DEI SYSTEM (DIFFRACTIVE ENERGY IMAGING SYSTEM), MID STREAM PREGNANCY TEST, ALTAIR MODEL, DEI SYSTEM (DIFFRACTIVE ENERGY IMAGING SYSTEM) and OS-2000 OPTICAL SONOGRAPHY SYSTEM.