De Ferris Laboratories, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Cytomegalovirus Igg Eia Kit Ref K880433
Regimes: 510(k) Registry: 510(k)Toxoplasma Gondii Igg Elisa Kit Ref K875258
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does De Ferris Laboratories, Inc. have in the registry?
The registry currently lists 2 devices for De Ferris Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list De Ferris Laboratories, Inc.'s devices?
Among its 2 most recently registered devices, De Ferris Laboratories, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do De Ferris Laboratories, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for De Ferris Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from De Ferris Laboratories, Inc. in the registry?
The most recently registered devices listed for De Ferris Laboratories, Inc. include CYTOMEGALOVIRUS IGG EIA KIT and TOXOPLASMA GONDII IGG ELISA KIT.