Sanyo North America Corp. is one of 25821 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sanyo North America Corp. - FDA 510(k) Cleared Devices
Recent clearances: SANYO CO2 INCUBATORS, MODELS NOS. MCO-17AC, MCO-17AIC, MCO-20AIC,AND MC0-175M
1
Total
1
Cleared
0
Denied
Sanyo North America Corp. has 1 FDA 510(k) cleared medical devices. Based in Tasca, US.
Historical record: 1 cleared submissions from 2001 to 2001. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Sanyo North America Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sanyo North America Corp.
1 devices