Spass, Inc. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Spass, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SpassageQ
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.
FDA 510(k) Regulatory Record - Spass, Inc.
1 devices