Allertec, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Amplified Elisa Ige Kit Ref K862368
Regimes: 510(k) Registry: 510(k)Rapid Specific Ige Procedure Ref K863394
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Allertec, Inc. have in the registry?
The registry currently lists 2 devices for Allertec, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Allertec, Inc.'s devices?
Among its 2 most recently registered devices, Allertec, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Allertec, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Allertec, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Allertec, Inc. in the registry?
The most recently registered devices listed for Allertec, Inc. include AMPLIFIED ELISA IGE KIT and RAPID SPECIFIC IGE PROCEDURE.