Telesair, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Telesair, Inc. has 2 FDA 510(k) cleared medical devices. Based in Irvine, US.
Latest FDA clearance: May 2025. Active since 2023. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Telesair, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by ProMedic Consulting, LLC and ProMedic, LLC.
2 devices