Belmont Instrument Corp. is one of 8384 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Belmont Instrument Corp. - FDA 510(k) Cleared Devices
Recent clearances: BELMONT HYPERTHERMIA PUMP, THE BELMONT BUDDY LITE FLUID WARMER, THE BELMONT FLUID MANAGEMENT SYSTEM/ THE BELMONT RAPID INFUSER, MODEL FMS2000
20
Total
19
Cleared
0
Denied
Belmont Instrument Corp. has 19 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 19 cleared submissions from 1981 to 2013. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Belmont Instrument Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Belmont Instrument Corp.
20 devices
Cleared
Nov 06, 2013
BELMONT HYPERTHERMIA PUMP
General Hospital
162d
Cleared
Nov 16, 2011
THE BELMONT BUDDY LITE FLUID WARMER
Hematology
65d
Cleared
Jul 01, 2009
THE BELMONT FLUID MANAGEMENT SYSTEM/ THE BELMONT RAPID INFUSER, MODEL FMS2000
General Hospital
8d
Cleared
Mar 26, 2009
THE BELMONT BUDDY LITE FLUID WARMER
Hematology
28d
Cleared
Feb 12, 2009
BELMONT HYPERTHERMIA PUMP
General Hospital
29d
Cleared
Jun 08, 2007
HYPERTHERMIA PUMP
General Hospital
91d
Cleared
Oct 19, 2006
BELMONT BUDDY PLUS FLUID WARMER
Hematology
31d
Cleared
Oct 13, 2005
BELMONT BUDDY FLUID WARMER
Hematology
27d
Cleared
Sep 22, 2003
LARGE VOLUME FLUID RESERVOIR
General Hospital
14d
Cleared
Sep 16, 2003
BELMONT FLUID MANAGEMENT SYSTEM, MODEL FMS2000
General Hospital
18d
Cleared
Jul 02, 2003
MICROHEATER
Hematology
51d
Cleared
Jan 06, 2000
BELMONT MODEL NGPBP INTRA-AORTIC BALLOON PUMP
Cardiovascular
430d