Medical Device Manufacturer · US , San Jose , CA

Visby Medical

2 submissions · 2 cleared · Since 2021
2
Total
2
Cleared
0
Denied

Visby Medical — FDA 510(k) Submissions

Visby Medical has submitted 2 FDA 510(k) premarket notifications since 2021, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Nucleic Acid Detection System For Non-viral Microorganism(s) Causing Sexually Transmitted Infections . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
Filters
All2 Microbiology 2