Argon Medical

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
28
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K130730V-STICK VASCULAR ACCESS SETNovember 22, 2013
K904994CLOSED SYSTEM FLUSH SETJanuary 15, 1991
K895511CATHETER BALLOON DILATOR PRESSURE GAUGEFebruary 28, 1990
K894157OBTURATORSeptember 28, 1989
K891022INTRODUCER FOR PTCA GUIDING CATHETERSMay 19, 1989
K884375TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETERJanuary 11, 1989
K882221OVER THE NEEDLE CATHETER, ARTERIAL CATHETER NEEDLEAugust 12, 1988
K871297KADIR HI-TORQUE GUIDE WIREApril 10, 1987
K853312ARGON CUT BIOPSY NEEDLES, VARIOUS SIZESSeptember 12, 1985
K852880PEEL-AWAY SHEATH(A COMPONENT OF ARGON INTROD SET)August 29, 1985
K844555PATHFINDER CARDIOVASCULAR CATHETERMarch 27, 1985
K842039ARGON DUAL LUMEN HEMODIALYSIS, CATHETERJanuary 29, 1985
K841926HYDROGLIDE SPRING GUIDE WIRESJanuary 2, 1985
K833303DUOFLO 6FDecember 27, 1983
K832030HEPARIN COATED STAINLESS STEEL/TEFLONSeptember 29, 1983
K831453SILCATH CENTRAL CATHETER TRAY W/18 GAJuly 28, 1983
K831451SILCATH CENTRAL CATHETER TRAY SIZE-June 8, 1983
K831171DIGICATHMay 25, 1983
K820883SEPTISLEEVEApril 29, 1982
K790353ACUTE RENAL DIALYSIS TRAYApril 20, 1979