Reimers Systems, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Reimers Systems, Inc. has 5 FDA 510(k) cleared medical devices. Based in Springfield, US.
Historical record: 5 cleared submissions from 1995 to 2011. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Reimers Systems, Inc. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Aug 19, 2011
RSI 4200
Anesthesiology
324d
Cleared
Oct 23, 1996
GSP1 - GAS SELECTION PANEL
Anesthesiology
92d
Cleared
Oct 23, 1996
ODS1 - HOOD DRIVER
Anesthesiology
92d
Cleared
Dec 15, 1995
T CLASS HYPERBARIC FACILITIES
Anesthesiology
118d
Cleared
Jun 02, 1995
LIFEFORCE CLINICAL HYPERBARIC FACILITY
Anesthesiology
81d