Diasonics Ultrasound
Country not established
- Devices
- 2
What Diasonics Ultrasound makes
Diasonics Ultrasound manufactures intraoperative ultrasound probes and the Masters Series 5000 ultrasound scanner, designed for real-time imaging during surgical procedures.
These devices are classified as Class II under FDA regulations and are listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Diasonics Itnraoperative Probes Ref K961002
Regimes: 510(k) Registry: 510(k)Diasonics Masters Series 5000 Ultrasound Scanner Ref K951998
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Diasonics Ultrasound have in the registry?
The registry currently lists 2 devices for Diasonics Ultrasound. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diasonics Ultrasound's devices?
Among its 2 most recently registered devices, Diasonics Ultrasound has devices listed in FDA 510(k) (2 devices).
What risk classes do Diasonics Ultrasound's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Diasonics Ultrasound's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Diasonics Ultrasound in the registry?
The most recently registered devices listed for Diasonics Ultrasound include DIASONICS ITNRAOPERATIVE PROBES and DIASONICS MASTERS SERIES 5000 ULTRASOUND SCANNER.