I.B. Bloxom C/O Hogan & Hartson is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
I.B. Bloxom C/O Hogan & Hartson - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
I.B. Bloxom C/O Hogan & Hartson has 1 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 1 cleared submissions from 1987 to 1987. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by I.B. Bloxom C/O Hogan & Hartson Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - I.B. Bloxom C/O Hogan & Hartson
1 devices