Acoustic Imaging
Country not established
- Devices
- 2
What Acoustic Imaging makes
Acoustic Imaging manufactures diagnostic ultrasound systems, including standalone transducers and Doppler-equipped units designed for medical imaging. These devices are intended for use in clinical settings to visualize internal body structures and assess blood flow, aiding in diagnostic procedures across various specialties.
The company’s portfolio is classified under FDA’s Class II regulatory category, with devices authorised through the 510(k) clearance pathway. These products are listed in the FDA’s 510(k) database and are based in the United States.
Catalogue
AI5200 Diagnostic Ultrasound System Transducer Ref K895071
Regimes: 510(k) Registry: 510(k)Ai 5200 Diagnostic Ultrasound System W/Doppler Ref K893833
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Acoustic Imaging have in the registry?
The registry currently lists 2 devices for Acoustic Imaging. Devices recorded under merged duplicate company entries are counted once.
Which registries list Acoustic Imaging's devices?
Among its 2 most recently registered devices, Acoustic Imaging has devices listed in FDA 510(k) (2 devices).
What risk classes do Acoustic Imaging's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Acoustic Imaging's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Acoustic Imaging in the registry?
The most recently registered devices listed for Acoustic Imaging include AI5200 DIAGNOSTIC ULTRASOUND SYSTEM TRANSDUCER and AI 5200 DIAGNOSTIC ULTRASOUND SYSTEM W/DOPPLER.