Revivant Corp.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Autopulse, Model 100 Ref K011046
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Autopulse Resuscitation System, Model 100 Ref K040453
Regimes: 510(k) Registry: 510(k)Autopulse Resuscitation System Ref K022345
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Revivant Corp. have in the registry?
The registry currently lists 4 devices for Revivant Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Revivant Corp.'s devices?
Among its 4 most recently registered devices, Revivant Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Revivant Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Revivant Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Revivant Corp. in the registry?
The most recently registered devices listed for Revivant Corp. include AUTOPULSE, MODEL 100, MODIFICATION TO: AUTOPULSE RESUSCITATION SYSTEM MODEL 100, AUTOPULSE RESUSCITATION SYSTEM, MODEL 100 and AUTOPULSE RESUSCITATION SYSTEM.