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 Gastroenterology & Urology ✕

5 devices

1-5 of 5

Cleared Jul 02, 1985

1070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERS

Gastroenterology & Urology · 68d

Cleared Jun 20, 1985

25-100,25-220 VARIOUS NEEDLE HOLDERS

Gastroenterology & Urology · 56d

Cleared Jun 20, 1985

25-230 TO 25-390 VARIOUS NEEDLE HOLDERS

Gastroenterology & Urology · 56d

Cleared May 23, 1985

53-100 TO 53-120 VARIOUS RECTAL SPECULA(SIMS, MATH

Gastroenterology & Urology · 28d

Cleared May 23, 1985

53-160 TO 53-167 VARIOUS BIOPSY FORCEPS YEOMAN

Gastroenterology & Urology · 28d