Mec/Surgitek Products is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mec/Surgitek Products - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Mec/Surgitek Products has 2 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 2 cleared submissions from 1983 to 1983. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Mec/Surgitek Products Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mec/Surgitek Products
2 devices