Bartels & Stout, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Test Kit For Detection Of Antinuclear Ref K802527
Regimes: 510(k) Registry: 510(k)Test Kit For Detection Of Herpes Simplex Ref K802526
Regimes: 510(k) Registry: 510(k)Direct Fluorescent Antibody Kit/Herpes Ref K802590
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bartels & Stout, Inc. have in the registry?
The registry currently lists 3 devices for Bartels & Stout, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bartels & Stout, Inc.'s devices?
Among its 3 most recently registered devices, Bartels & Stout, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Bartels & Stout, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Bartels & Stout, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bartels & Stout, Inc. in the registry?
The most recently registered devices listed for Bartels & Stout, Inc. include TEST KIT FOR DETECTION OF ANTINUCLEAR, TEST KIT FOR DETECTION OF HERPES SIMPLEX and DIRECT FLUORESCENT ANTIBODY KIT/HERPES.