Acuson Corp.
United StatesFDA applicant, unverified
- Devices
- 37
What Acuson Corp. makes
Acuson Corp. manufactures diagnostic ultrasound systems, including the Sequoia Signature II and Cypress systems, along with specialized transducers like the S228 for transcranial Doppler and V714OR for imaging. Their portfolio also includes needle guides, such as the Quick-Clip, and software tools like the CSV12 Viewer for image analysis. Additional offerings include harmonic imaging with contrast agents, 3D organ assessment with magnetic position sensing, and system modifications for archiving and communication.
The company’s devices are regulated under FDA’s 510(k) pathway and fall into Class I and Class II classifications. Products are listed in the FDA’s 510(k) database, indicating they meet applicable U.S. regulatory requirements. Acuson Corp. is based in the United States.
Catalogue
Search and filter all 37 devicesFrequently asked questions
How many devices does Acuson Corp. have in the registry?
The registry currently lists 37 devices for Acuson Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Acuson Corp.'s devices?
Among its 37 most recently registered devices, Acuson Corp. has devices listed in FDA 510(k) (37 devices).
What risk classes do Acuson Corp.'s devices fall under?
Among its 37 most recently registered devices, the classes recorded for Acuson Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Acuson Corp. in the registry?
The most recently registered devices listed for Acuson Corp. include CYPRESS SYSTEM, QUICK-CLIP NEEDLE GUIDE, ACUSON PICTURE ARCHIVING & COMMUNICATION SYSTEM MODIFICATION and ACUSON MODEL 3001.