Dobre, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Dobre, Inc. makes
Dobre, Inc. manufactures electrocardiographic electrodes and the PLEXUS PULSER I and PLEXUS PULSER II devices.
These products are Class II devices listed in the FDA 510(k) registry, and the company is based in the US.
Catalogue
Plexus Pulser I, Plexus Pulser Ii Ref K924891
510(k) 510(k)Electrocardiographic Electrodes, Disp. Ref K770521
510(k) 510(k)
Frequently asked questions
How many devices does Dobre, Inc. have in the registry?
The registry currently lists 2 devices for Dobre, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dobre, Inc.'s devices?
Among its 2 most recently registered devices, Dobre, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Dobre, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Dobre, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dobre, Inc. in the registry?
The most recently registered devices listed for Dobre, Inc. include PLEXUS PULSER I, PLEXUS PULSER II and ELECTROCARDIOGRAPHIC ELECTRODES, DISP..