Scanlan Intl., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
19
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K960372SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEMApril 26, 1996
K945474SCANLAN(R) THORACOSCOPIC SCISSORS, CLAMP, FORCEPS, NEEDLE HOLDERDecember 5, 1994
K911184SCANLAN/TAHERI VALVULOTOMEFebruary 18, 1992
K864920SCANLAN (TM) INSTRUMENT TRAYJanuary 12, 1987
K864919SCANLAN (TM) VEIN/GRAFT HOLDERJanuary 12, 1987
K851825SCANLAN TUNNELER, SHEATH & TIPJuly 12, 1985
K841521SCANLAN ENDARSECTORAugust 3, 1984
K841513SCANLAN ATRAUM INSTRUMENT JAW COVERJuly 6, 1984
K841085SCANLAN COLORMARK SKIN MARKERJune 11, 1984
K841515SCANLAN VASCU-STATT IIJune 5, 1984
K841514SCANLAN VASCU-STATT II APPROXIMATORJune 5, 1984
K841086SURGICAL INSTRUMENT DEMAGNETIZERApril 24, 1984
K823764SCANLAN SINGLE-USE AORTA PUNCHMarch 24, 1983
K823694VASCU-STATT APPROXIMATORJanuary 7, 1983
K821887SCANLAN SUTURE-STATTJuly 28, 1982
K810480SCANLAN SUTURE BOOTSMarch 13, 1981
K802829SCANLAN VASCU-STATTJanuary 15, 1981
K801976SCANLAN STERNUM NEEDLE-SUTURESeptember 26, 1980
K780255NEEDLE DRIVERApril 18, 1978