Browne Medical, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
What Browne Medical, Inc. makes
Browne Medical, Inc. makes urodynamic monitoring systems and related devices, including the Urometer, Urobei Stress Incontinence Monitor, Profile Urodynamic Monitoring System, and Bedside N.P.T. 9900 with Printer 9800.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Urometer Ref K833043
510(k) 510(k)Urobei Stress Incontinence Monitor Ref K851483
510(k) 510(k)Profile Urodynamic Monitoring Sys Ref K834503
510(k) 510(k)Bedside N.P.T. 9900 - Printer 9800 Ref K830221
510(k) 510(k)
Frequently asked questions
How many devices does Browne Medical, Inc. have in the registry?
The registry currently lists 4 devices for Browne Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Browne Medical, Inc.'s devices?
Among its 4 most recently registered devices, Browne Medical, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Browne Medical, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Browne Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Browne Medical, Inc. in the registry?
The most recently registered devices listed for Browne Medical, Inc. include UROMETER, UROBEI STRESS INCONTINENCE MONITOR, PROFILE URODYNAMIC MONITORING SYS and BEDSIDE N.P.T. 9900 - PRINTER 9800.