U.S. Imaging, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
What U.S. Imaging, Inc. makes
U.S. Imaging, Inc. manufactures hardware interfaces and control units for fluoroscopic and X-ray imaging systems, including photomultiplier tube interface boards, remote fluoroscopic controls, and modified X-ray control panels for specific models like the ED125L and ED150L. Their portfolio also includes pulsed fluoroscopic control units designed to enhance imaging workflows in medical settings.
The company’s devices are classified under FDA regulations as Class I and Class II, with relevant submissions recorded in the FDA’s 510(k) clearance database. These products are intended for use in radiology environments and comply with U.S. medical device authorization requirements.
Catalogue
Photomulitplier Tube Interface P.C. Board Ref K890878
510(k) 510(k)U.S.I. Model 1012, Remote Fluoroscopic Control Ref K900062
510(k) 510(k)Pulsed Fluoroscopic Control Model:pf-02 Ref K882358
510(k) 510(k)Modified X-Ray Controls, Model ED125L And ED150L Ref K881886
510(k) 510(k)
Frequently asked questions
How many devices does U.S. Imaging, Inc. have in the registry?
The registry currently lists 4 devices for U.S. Imaging, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list U.S. Imaging, Inc.'s devices?
Among its 4 most recently registered devices, U.S. Imaging, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do U.S. Imaging, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for U.S. Imaging, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from U.S. Imaging, Inc. in the registry?
The most recently registered devices listed for U.S. Imaging, Inc. include PHOTOMULITPLIER TUBE INTERFACE P.C. BOARD, U.S.I. MODEL 1012, REMOTE FLUOROSCOPIC CONTROL, PULSED FLUOROSCOPIC CONTROL MODEL:PF-02 and MODIFIED X-RAY CONTROLS, MODEL ED125L AND ED150L.