Browne Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 7
What Browne Corp. makes
Browne Corp. manufactures Class II medical devices, including the CF-1 and CF-1G models for specific clinical applications, as well as UA-6 units for diagnostic or procedural use. The GD-5 model serves a distinct purpose in patient monitoring or treatment, while the UD-4 series (UD-4DE, UD-4D, UD-4, UD-4E) appears tailored for ultrasound-guided procedures or imaging.
These devices are regulated under the US FDA’s 510(k) pathway as Class II products and are listed in the FDA’s 510(k) database. Browne Corp. is based in the United States.
Catalogue
Browne Model Cf-1 And Cf-1g Ref K790754
510(k) 510(k)Browne Model Ua-6 Ref K792094
510(k) 510(k)Browne Model Gd-5 Ref K792093
510(k) 510(k)Browne Model Ud-4DE Ref K790478
510(k) 510(k)Browne Model Ud-4D Ref K792091
510(k) 510(k)Browne Model Ud-4 Ref K792090
510(k) 510(k)Browne Model Ud-4E Ref K792092
510(k) 510(k)
Frequently asked questions
How many devices does Browne Corp. have in the registry?
The registry currently lists 7 devices for Browne Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Browne Corp.'s devices?
Among its 7 most recently registered devices, Browne Corp. has devices listed in FDA 510(k) (7 devices).
What risk classes do Browne Corp.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Browne Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Browne Corp. in the registry?
The most recently registered devices listed for Browne Corp. include BROWNE MODEL CF-1 AND CF-1G, BROWNE MODEL UA-6, BROWNE MODEL GD-5 and BROWNE MODEL UD-4DE.