American Science and Engineering, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What American Science and Engineering, Inc. makes
American Science and Engineering, Inc. manufactures dual-gantry digital radiography systems, whole-body X-ray scanners, and computerized tomographic X-ray scanners for medical imaging applications.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Digital Radiography Sys Dual Gantries Ref K833237
Regimes: 510(k) Registry: 510(k)X-Ray Scanner, Whole Body, As&E Ref K761004
Regimes: 510(k) Registry: 510(k)X-Ray Scanner, Computerized Tomographic Ref K760201
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Science and Engineering, Inc. have in the registry?
The registry currently lists 3 devices for American Science and Engineering, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Science and Engineering, Inc.'s devices?
Among its 3 most recently registered devices, American Science and Engineering, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do American Science and Engineering, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for American Science and Engineering, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Science and Engineering, Inc. in the registry?
The most recently registered devices listed for American Science and Engineering, Inc. include DIGITAL RADIOGRAPHY SYS DUAL GANTRIES, X-RAY SCANNER, WHOLE BODY, AS&E and X-RAY SCANNER, COMPUTERIZED TOMOGRAPHIC.