Aller-Screen, Inc.
Country not established
- Devices
- 1
What Aller-Screen, Inc. makes
Aller-Screen, Inc. manufactures the ALLER-SCREEN SKIN TEST KIT, a diagnostic device used for identifying allergic reactions through skin testing procedures.
The device falls under FDA Class II regulation and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Aller-Screen Skin Test Kit Ref K791328
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aller-Screen, Inc. have in the registry?
The registry currently lists 1 device for Aller-Screen, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aller-Screen, Inc.'s devices?
Among its 1 most recently registered device, Aller-Screen, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Aller-Screen, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Aller-Screen, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aller-Screen, Inc. in the registry?
The most recently registered devices listed for Aller-Screen, Inc. include ALLER-SCREEN SKIN TEST KIT.