Ross Research, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Ross Research, Inc. makes
Ross Research, Inc. manufactures non-invasive temporary pacemakers and pacemaker pulse generators with integrated electrodes, designed for short-term cardiac rhythm management.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Noninvasive Temporary Pacemaker Ref K822246
Regimes: 510(k) Registry: 510(k)Pacemaker Pulse Generator W/Electrode Ref K840353
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ross Research, Inc. have in the registry?
The registry currently lists 2 devices for Ross Research, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ross Research, Inc.'s devices?
Among its 2 most recently registered devices, Ross Research, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Ross Research, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ross Research, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ross Research, Inc. in the registry?
The most recently registered devices listed for Ross Research, Inc. include NONINVASIVE TEMPORARY PACEMAKER and PACEMAKER PULSE GENERATOR W/ELECTRODE.