Verathon Incorporated
United StatesFDA applicant, unverified
- Devices
- 5
What Verathon Incorporated makes
Verathon Incorporated manufactures bladder ultrasound systems, including portable and handheld devices like the BladderScan BVI 9400, BVM 9500, and BladderScan Prime Series. These devices measure residual urine volume in patients post-voiding, aiding clinical assessments in bladder management.
The company’s ultrasound systems are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearances. The portfolio is listed in the FDA’s 510(k) database, reflecting regulatory authorisation for these diagnostic tools. Verathon Incorporated is headquartered in the United States.
Catalogue
Bladderscan Bvi 9400 Ultrasound Ref K071217
Regimes: 510(k) Registry: 510(k)Verathon Inc. Bladderscan Bvm 9500 Ultrasound Ref K090214
Regimes: 510(k) Registry: 510(k)BladderScan Prime System Ref K153101
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
BladderScan Prime PLUS System Ref K172356
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Verathon Incorporated have in the registry?
The registry currently lists 5 devices for Verathon Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Verathon Incorporated's devices?
Among its 5 most recently registered devices, Verathon Incorporated has devices listed in FDA 510(k) (5 devices).
What risk classes do Verathon Incorporated's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Verathon Incorporated's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Verathon Incorporated in the registry?
The most recently registered devices listed for Verathon Incorporated include BLADDERSCAN BVI 9400 ULTRASOUND, VERATHON INC. BLADDERSCAN BVM 9500 ULTRASOUND, BladderScan Prime System and VERATHON INC. BLADDERSCAN ULTRASOUND SYSTEM, MODEL BVI 9600.