Erich Jaeger, Inc. - FDA 510(k) Cleared Devices
28
Total
28
Cleared
0
Denied
Erich Jaeger, Inc. has 28 FDA 510(k) cleared anesthesiology devices. Based in Rockford, US.
Historical record: 28 cleared submissions from 1984 to 2000.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
28 devices
Cleared
Dec 27, 2000
APNOESCREEN PRO, ALPHA SCREEN PRO
Anesthesiology
324d
Cleared
Apr 30, 1998
TOENNIES NEUROSCREEN SYSTEM
Neurology
307d
Cleared
Sep 20, 1996
ASTHMA MONITOR
Anesthesiology
259d
Cleared
Mar 07, 1994
FLOWSCREEN
Anesthesiology
272d
Cleared
Mar 07, 1994
MASTER SCREEN PNUEMO
Anesthesiology
214d
Cleared
Feb 21, 1986
ALVEO-DIFFUSION TEST
Anesthesiology
189d
Cleared
Feb 05, 1986
INFANT BODY TEST
Anesthesiology
176d
Cleared
Feb 05, 1986
SCREENMATE
Anesthesiology
177d
Cleared
Feb 05, 1986
ERGO-PNEUMOTEST
Anesthesiology
174d
Cleared
Sep 03, 1985
N20 TEST
Anesthesiology
22d
Cleared
Jul 01, 1985
PNEUMOSCOPE
Anesthesiology
31d
Cleared
Feb 14, 1985
UNIVERSAL-BODYTEST
Anesthesiology
136d