Medical Device Manufacturer · US , Mahwah , NJ

Philips Hearing Instruments Co. - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 1991
20
Total
20
Cleared
0
Denied

Philips Hearing Instruments Co. has 20 FDA 510(k) cleared ear, nose, throat devices. Based in Mahwah, US.

Historical record: 20 cleared submissions from 1991 to 1997.

Browse the complete list of FDA 510(k) cleared ear, nose, throat devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Philips Hearing Instruments Co.

20 devices
1-12 of 20
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