Stasis Labs, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stasis Labs, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Stasis Monitoring System
1
Total
1
Cleared
0
Denied
Stasis Labs, Inc. has 1 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Stasis Labs, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by 510konsult, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Stasis Labs, Inc.
1 devices