Stanco Medical, Inc. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Stanco Medical, Inc. has 19 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 19 cleared submissions from 1979 to 1981.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stanco Medical, Inc.
19 devices
Cleared
Apr 08, 1981
ATRIAL-VENTRICULAR PACING ELECTRODE KIT
Cardiovascular
29d
Cleared
Apr 08, 1981
UNIVERSAL PACING ELECTRODE KIT
Cardiovascular
29d
Cleared
Nov 26, 1980
PERICARDIOCENTESIS KIT
Toxicology
68d
Cleared
Nov 20, 1980
RIGHT ATRIAL LINE KIT
Cardiovascular
62d
Cleared
Nov 20, 1980
SWAN GANZ CATHETER PLACEMENT KIT
Cardiovascular
62d
Cleared
Oct 23, 1980
TRANSVENOUS PACEMAKER ELECTRODE KIT
Cardiovascular
37d
Cleared
Oct 17, 1980
REGIONAL INTRAVENOUS ANESTHESIA KIT
Anesthesiology
28d
Cleared
Oct 10, 1980
VASCULAR CATHETER WIREGUIDES
Cardiovascular
24d
Cleared
Oct 10, 1980
PRESSURE MONITORING LINES
Cardiovascular
17d
Cleared
Oct 10, 1980
SHEATH DILATOR SET
Cardiovascular
17d
Cleared
Oct 10, 1980
DISP. TOUGY-BORST TYPE ADAPTOR W/PORT
Cardiovascular
17d
Cleared
Oct 03, 1980
PRESSURE GAUGE ACCESSORY KIT/DILATATION
Cardiovascular
17d