Laurie Ann Kaiser, Ph.D.
Country not established
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Peritone Ref K800191
Regimes: 510(k) Registry: 510(k)Peritone Disposal Sheath - Rubber And Vinyl Ref K860552
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Laurie Ann Kaiser, Ph.D. have in the registry?
The registry currently lists 2 devices for Laurie Ann Kaiser, Ph.D.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Laurie Ann Kaiser, Ph.D.'s devices?
Among its 2 most recently registered devices, Laurie Ann Kaiser, Ph.D. has devices listed in FDA 510(k) (2 devices).
What risk classes do Laurie Ann Kaiser, Ph.D.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Laurie Ann Kaiser, Ph.D.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Laurie Ann Kaiser, Ph.D. in the registry?
The most recently registered devices listed for Laurie Ann Kaiser, Ph.D. include PERITONE and PERITONE DISPOSAL SHEATH - RUBBER AND VINYL.