Erich Jaeger GmbH - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Erich Jaeger GmbH has 5 FDA 510(k) cleared medical devices. Based in Yorba Linda, US.
Historical record: 5 cleared submissions from 2000 to 2003. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Erich Jaeger GmbH Filter by specialty or product code using the sidebar.
5 devices
Cleared
Nov 12, 2003
OXYCON MOBILE
Anesthesiology
419d
Cleared
Mar 03, 2003
MS PAED-BABY BODY
Anesthesiology
110d
Cleared
Feb 12, 2003
SLEEPSCREEN/APNOESCREEN CARDIO
Anesthesiology
309d
Cleared
Jul 12, 2000
AEROSOL PROVOCATION SYSTEM APS PRO, MODEL APS PRO
Anesthesiology
58d
Cleared
Mar 29, 2000
SPIRO PRO
Anesthesiology
30d