Hospitech Respiration , Ltd. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Hospitech Respiration , Ltd. has 6 FDA 510(k) cleared medical devices. Based in Binyamina, IL.
Last cleared in 2022. Active since 2010. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Hospitech Respiration , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Hospitech Respiration , Ltd.
6 devices
Cleared
Dec 29, 2022
AG100s
Anesthesiology
220d
Cleared
Oct 12, 2018
AG 100s
Anesthesiology
179d
Cleared
Feb 16, 2016
AnapnoGuard 100 Respiratory Guard System
Anesthesiology
389d
Cleared
May 13, 2013
AG MASS
General & Plastic Surgery
24d
Cleared
May 03, 2013
AG GUFFILL
Anesthesiology
240d
Cleared
Mar 02, 2010
ANAPNOGUARD ENDOTRACHEAL TUBE
Anesthesiology
151d