Electromedics, Inc. - FDA 510(k) Cleared Devices
41
Total
41
Cleared
0
Denied
Electromedics, Inc. has 41 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 41 cleared submissions from 1977 to 1994. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Electromedics, Inc. Filter by specialty or product code using the sidebar.
41 devices
Cleared
Mar 07, 1994
ELECTROMEDICS TYMPANIC TEMPERATURE SENSOR
General Hospital
143d
Cleared
Jan 28, 1994
ELECTROMEDICS HG (HYDROGEL) SERIES SKIN TEMPERATURE SENSOR
General Hospital
176d
Cleared
Dec 03, 1993
ELECTROMEDICS BLOOD HEAT EXCHANGER
Cardiovascular
87d
Cleared
Jul 01, 1993
EL2-SERIES BLOOD COLLECTION REERVOIR
Cardiovascular
169d
Cleared
Feb 19, 1993
ELECTROMEDICS EL-SERIES CARDIOTOMY RESERVOIR
Cardiovascular
67d
Cleared
Feb 05, 1993
ELECTROMEDICS TISSUE TRAP/ #TT280
General Hospital
102d
Cleared
Sep 03, 1992
AUTOTRANSFUSION BLOOD COLLECTION RESERVOIR
Cardiovascular
258d
Cleared
Jun 19, 1991
PORTABLE AUTO TRANSFUSION SYSTEM 500
Anesthesiology
152d
Cleared
May 16, 1991
MODIFIED PYROGEN TESTING
Cardiovascular
91d
Cleared
Dec 13, 1990
ARTERIAL BLOOD FILTER ELECTRO. AIR* STAR 40 AND 20
Cardiovascular
177d
Cleared
Sep 06, 1990
ELECTROMEDICS BT422-120 AND BT422-40
Anesthesiology
41d
Cleared
Jun 12, 1990
AP900/PRP MODULE AND ACCESSORIES, MODIFICATION
Anesthesiology
411d
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