Medical Device Manufacturer · US , Framingham , MA

Bose Corporation

2 submissions · 1 cleared · Since 2018
2
Total
1
Cleared
1
Denied

Bose Corporation — FDA 510(k) Submissions

Bose Corporation has submitted 2 FDA 510(k) premarket notifications since 2018, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Self-fitting Air-conduction Hearing Aid, Prescription . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Ear, Nose, Throat 2