Scanlan Intl., Inc. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
FDA 510(k) Regulatory Record - Scanlan Intl., Inc. Cardiovascular ✕
5 devices
Cleared
Feb 18, 1992
SCANLAN/TAHERI VALVULOTOME
Cardiovascular
337d
Cleared
Jan 12, 1987
SCANLAN (TM) VEIN/GRAFT HOLDER
Cardiovascular
27d
Cleared
Jul 12, 1985
SCANLAN TUNNELER, SHEATH & TIP
Cardiovascular
77d
Cleared
Aug 03, 1984
SCANLAN ENDARSECTOR
Cardiovascular
113d
Cleared
Mar 24, 1983
SCANLAN SINGLE-USE AORTA PUNCH
Cardiovascular
100d