Ark Surgical, Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Ark Surgical, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Nazareth, IL.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ark Surgical, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by ProMedoss, Inc. as regulatory consultant.
1 devices