Arch Development Group
Country not established
- Devices
- 2
What Arch Development Group makes
Arch Development Group manufactures the Stasis Button Pressure Device, a medical tool designed to manage edema and promote fluid redistribution in patients, and the Sterilesert™ Cable and Pole Drape, a sterile barrier used in medical procedures to protect cables and poles from contamination.
The company’s products are regulated under FDA’s 510(k) pathway, with devices classified as Class I and Class II. They are listed in the FDA’s 510(k) database and are based in the United States.
Catalogue
Stasis Button Prssure Device Ref K912765
Regimes: 510(k) Registry: 510(k)Sterilesert(Tm) Cable And Pole Drape Ref K913047
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arch Development Group have in the registry?
The registry currently lists 2 devices for Arch Development Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arch Development Group's devices?
Among its 2 most recently registered devices, Arch Development Group has devices listed in FDA 510(k) (2 devices).
What risk classes do Arch Development Group's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Arch Development Group's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Arch Development Group in the registry?
The most recently registered devices listed for Arch Development Group include STASIS BUTTON PRSSURE DEVICE and STERILESERT(TM) CABLE AND POLE DRAPE.