Enthermics Medical Systems, Inc. is one of 20677 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Enthermics Medical Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DC SERIES FLUID WARMING CABINET, DC SERIES FLUID WARMING CABINET, IVNOW MODULAR FLUID WARMER, 120V, MODEL IVNOW-1, IVNOW-2, IVNOW-3, IVNOW-6, IVNOW MODULAR FLUID WARMER 230V, EC-7701 FLUID WARMING CABINET
4
Total
4
Cleared
0
Denied
Enthermics Medical Systems, Inc. has 4 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 4 cleared submissions from 1997 to 2013. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Enthermics Medical Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Enthermics Medical Systems, Inc.
4 devices
Cleared
Dec 06, 2013
DC SERIES FLUID WARMING CABINET, DC SERIES FLUID WARMING CABINET
General Hospital
143d
Cleared
May 07, 2010
IVNOW MODULAR FLUID WARMER, 120V, MODEL IVNOW-1, IVNOW-2, IVNOW-3, IVNOW-6,...
General Hospital
366d
Cleared
Jan 20, 2000
EC-7701 FLUID WARMING CABINET
General & Plastic Surgery
72d
Cleared
Apr 22, 1997
TRU-5000 THERMAL RECOVERY RADIANT HEATING UNIT
Cardiovascular
217d