Stihler Electronic GmbH - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Stihler Electronic GmbH has 6 FDA 510(k) cleared medical devices. Based in Sound Beach, US.
Historical record: 6 cleared submissions from 1999 to 2020.
Browse the FDA 510(k) cleared devices submitted by Stihler Electronic GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Stihler Electronic GmbH
6 devices
Cleared
Sep 04, 2020
Astopad Patient Warming System
Cardiovascular
30d
Cleared
Dec 19, 2008
PRISMAFLO II
Gastroenterology & Urology
91d
Cleared
Dec 18, 2008
ASTOFLO PLUS
General Hospital
87d
Cleared
Jul 24, 2002
PRISMAFLO
Gastroenterology & Urology
194d
Cleared
Sep 03, 1999
PRISMATHERM II, ASTOLINE
Hematology
149d
Cleared
Sep 02, 1999
ASTOTHERM PLUS, ASTOTUBES, ASTOLINE
Hematology
148d