Medasonics, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 19
What Medasonics, Inc. makes
Medasonics, Inc. manufactures diagnostic ultrasound systems, including the Cadence Doppler Ultrasound System and TransPect Transcranial Doppler, as well as vascular assessment tools like the Vasculab Bi-Directional Doppler and Vasculab Spectrum Analyzer. The company also produces peripheral vascular diagnostic devices, such as the Plethysmograph with Strain Gauge, Sequential Cuff Inflation Devices, and the Medacord Personal Vascular Laboratory. Additional products include the Cerebrovascular Diagnostic System, TED Sequential Compression Devices for limb circulation, and the ObTrasound Stethoscope for fetal monitoring.
The company’s devices are classified under FDA regulations as Class I and Class II, with submissions recorded in the FDA’s 510(k) clearance registry. These products are intended for vascular, neurological, and fetal diagnostic applications, adhering to U.S. medical device compliance standards. Medasonics, Inc. is based in the United States.
Catalogue
Search and filter all 19 devicesFrequently asked questions
How many devices does Medasonics, Inc. have in the registry?
The registry currently lists 19 devices for Medasonics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medasonics, Inc.'s devices?
Among its 19 most recently registered devices, Medasonics, Inc. has devices listed in FDA 510(k) (19 devices).
What risk classes do Medasonics, Inc.'s devices fall under?
Among its 19 most recently registered devices, the classes recorded for Medasonics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medasonics, Inc. in the registry?
The most recently registered devices listed for Medasonics, Inc. include CADENCE DOPPLER ULTRASOUND SYSTEM, TRANSPECT TRANSCRANIAL DOPPLER, PLETHYSMOGRAPH, STRAIN GAUGE and VASCULAB #R12B.