Breas Medical AB - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Breas Medical AB has 15 FDA 510(k) cleared anesthesiology devices. Based in Molnlycke, Vastra Gotaland, SE.
Latest FDA clearance: May 2025. Active since 2006.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Breas Medical AB
15 devices
Cleared
May 20, 2025
EveryWare
Anesthesiology
272d
Cleared
May 16, 2025
Clearo
Anesthesiology
273d
Cleared
Jan 13, 2025
Vivo 45 LS
Anesthesiology
451d
Cleared
Dec 13, 2024
Vivo 1, Vivo 2
Anesthesiology
267d
Cleared
Dec 13, 2024
Vivo 3
Anesthesiology
267d
Cleared
Jan 27, 2021
Vivo 45 LS
Anesthesiology
401d
Cleared
Nov 09, 2016
Vivo 60
Anesthesiology
261d
Cleared
May 14, 2009
BREAS VIVO 40 SYSTEM
Anesthesiology
113d
Cleared
Feb 15, 2008
BREAS VIVO BILEVEL SYSTEM, MODEL VIVO 40
Anesthesiology
239d
Cleared
Jan 22, 2007
BREAS ISLEEP 20I
Anesthesiology
67d
Cleared
Aug 18, 2006
ISLEEP BY BREAS, MODELS ISLEEP 10, ISLEEP 20.
Anesthesiology
158d
Cleared
Jun 23, 2006
BREAS ISLEEP 20+
Anesthesiology
67d