Strados Labs is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Strados Labs - FDA 510(k) Cleared Devices
Recent clearances: Strados Remote Electronic Stethoscope Platform (RESP)
1
Total
1
Cleared
0
Denied
Strados Labs has 1 FDA 510(k) cleared medical devices. Based in Philadelphia, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Strados Labs Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Powers Regulatory Consulting/64954 as regulatory consultant.
FDA 510(k) Regulatory Record - Strados Labs
1 devices