Medical Device Manufacturer · US , San Antonio , TX

Artiberia - FDA 510(k) Cleared Devices

79 submissions · 79 cleared · Since 1985

79

Total

79

Cleared

0

Denied

FDA 510(k) Regulatory Record - Artiberia Ophthalmic ✕

4 devices

1-4 of 4

Cleared Jun 20, 1985

13-550,13-560 WESCOTT SCOSSORS (EYE)

Ophthalmic · 56d

Cleared May 30, 1985

37-610 TO 37-880 VARIOUS OPHTHAL-FORCEPS

Ophthalmic · 35d

Cleared May 30, 1985

37-940 TO 37-944 VARIOUS NOYES OPHTHALMIC FORCEPS

Ophthalmic · 35d

Cleared May 23, 1985

37-200 TO 37-246 VARIOUS OPHTHALMOLOGY SCALPELS/KN

Ophthalmic · 28d