Breathesuite, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Breathesuite, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BreatheSuite MDI V1
1
Total
1
Cleared
0
Denied
Breathesuite, Inc. has 1 FDA 510(k) cleared medical devices. Based in St. John'S, CA.
Last cleared in 2021. Active since 2021. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Breathesuite, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Breathesuite, Inc.
1 devices