Spass, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Spass, Inc. has 1 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Last cleared in 2023. Active since 2023. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Spass, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Radios, LLC as regulatory consultant.
1 devices