Arrow X-Ray Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Arrow X-Ray Corp. makes
Arrow X-Ray Corp. manufactures the Podioscope, a portable X-ray imaging device designed for podiatric examinations. The device is intended for capturing high-quality images of feet and lower extremities, aiding in the diagnosis of bone and soft tissue conditions.
The Podioscope falls under FDA Class II regulation and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Podioscope By Arrow Ref K827069
Regimes: 510(k) Registry: 510(k)Podioscope By Arrow Ref K820119
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arrow X-Ray Corp. have in the registry?
The registry currently lists 2 devices for Arrow X-Ray Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arrow X-Ray Corp.'s devices?
Among its 2 most recently registered devices, Arrow X-Ray Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Arrow X-Ray Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Arrow X-Ray Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Arrow X-Ray Corp. in the registry?
The most recently registered devices listed for Arrow X-Ray Corp. include PODIOSCOPE BY ARROW.