Medical Device Manufacturer · DK , Denmark

New Brillette A/S - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1985

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - New Brillette A/S Ophthalmic ✕

1 devices

1-1 of 1

Cleared May 30, 1985

SPECTACLE FRAME

Ophthalmic · 70d