Performance Ent.
CanadaFDA applicant, unverified
- Devices
- 1
What Performance Ent. makes
Performance Ent. manufactures the DynaVision 2000, a Class U medical device designed for diagnostic imaging, likely intended for specific radiographic or fluoroscopic applications.
The DynaVision 2000 is regulated under the FDA’s 510(k) pathway and is listed in the U.S. as a Class U device. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Dynavision 2000 Ref K911938
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Performance Ent. have in the registry?
The registry currently lists 1 device for Performance Ent.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Performance Ent.'s devices?
Among its 1 most recently registered device, Performance Ent. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Performance Ent. in the registry?
The most recently registered devices listed for Performance Ent. include DYNAVISION 2000.