Rohe Scientific Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Rohe Scientific Corp. makes
Rohe Scientific Corp. manufactures the Primus Inter Paresechocardiography System, a diagnostic imaging device used for echocardiographic evaluations, and digital ultrasound systems for medical diagnostics.
These products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Rohnar 7000 Digital Diagn Ultrasound Ref K791505
Regimes: 510(k) Registry: 510(k)Primus Inter Paresechocardiography Sys. Ref K770073
Regimes: 510(k) Registry: 510(k)Digital Diagnostic Ultrasound Device Ref K810038
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rohe Scientific Corp. have in the registry?
The registry currently lists 3 devices for Rohe Scientific Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rohe Scientific Corp.'s devices?
Among its 3 most recently registered devices, Rohe Scientific Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Rohe Scientific Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Rohe Scientific Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rohe Scientific Corp. in the registry?
The most recently registered devices listed for Rohe Scientific Corp. include ROHNAR 7000 DIGITAL DIAGN ULTRASOUND, PRIMUS INTER PARESECHOCARDIOGRAPHY SYS. and DIGITAL DIAGNOSTIC ULTRASOUND DEVICE.