Mediscra, Inc.
Country not established
- Devices
- 1
What Mediscra, Inc. makes
Mediscra, Inc. manufactures ultrasound scanners designed for imaging the body and heart, enabling diagnostic evaluations in clinical settings.
These devices are regulated under the FDA’s 510(k) pathway as Class II medical devices and are listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Scanner, Ultrasound Body/Heart Ref K760223
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mediscra, Inc. have in the registry?
The registry currently lists 1 device for Mediscra, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mediscra, Inc.'s devices?
Among its 1 most recently registered device, Mediscra, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Mediscra, Inc. in the registry?
The most recently registered devices listed for Mediscra, Inc. include SCANNER, ULTRASOUND BODY/HEART.