Iba/Griffith is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Iba/Griffith - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Iba/Griffith has 1 FDA 510(k) cleared medical devices. Based in Monument, US.
Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Iba/Griffith Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Iba/Griffith
1 devices