Marks & Murase is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Marks & Murase - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Marks & Murase has 3 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 3 cleared submissions from 1994 to 1995. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Marks & Murase Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Marks & Murase
3 devices