O.R. Solutions, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
O.R. Solutions, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
O.R. Solutions, Inc. has 7 FDA 510(k) cleared medical devices. Based in Chantilly, US.
Historical record: 7 cleared submissions from 1995 to 2005. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by O.R. Solutions, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - O.R. Solutions, Inc.
7 devices
Cleared
Aug 30, 2005
ORS MODEL 6000 ENDOSCOPE HOLDER
Gastroenterology & Urology
40d
Cleared
Nov 13, 2002
ORS-3000LD
General Hospital
43d
Cleared
Nov 13, 2002
1075LD HUSH-SLUSH
General Hospital
43d
Cleared
Jun 27, 2002
ORS-1000LD
General Hospital
65d
Cleared
Jun 26, 2002
WARMER 2000LD
General Hospital
64d
Cleared
Sep 12, 1996
DMS-9000
General Hospital
196d
Cleared
Sep 22, 1995
ORS-111
General Hospital
51d