Sonorous NV, Inc.
United Statesfrom the FDA registration address FDA FEI 3047894544
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Sonorous NV, Inc. makes
Sonorous NV, Inc. manufactures the BosCATH Support Catheter, a device designed for use in medical procedures requiring catheter support.
The BosCATH Support Catheter is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
BosCATH Support Catheter Ref K254046
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3047894544
- Address
- 1 Spectrum Pointe Dr., Lake Forest, CA, 92630
Frequently asked questions
How many devices does Sonorous NV, Inc. have in the registry?
The registry currently lists 1 device for Sonorous NV, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sonorous NV, Inc.'s devices?
Among its 1 most recently registered device, Sonorous NV, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sonorous NV, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sonorous NV, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sonorous NV, Inc. in the registry?
The most recently registered devices listed for Sonorous NV, Inc. include BosCATH Support Catheter.