Hospi Corporation is one of 16079 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hospi Corporation - FDA 510(k) Cleared Devices
Recent clearances: MACY CATHETER
1
Total
1
Cleared
0
Denied
Hospi Corporation has 1 FDA 510(k) cleared medical devices. Based in Concord, US.
Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Hospi Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Hospi Corporation
1 devices