Medtronic Cryocath, LP

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
7
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K202620FlexCath Advance Steerable Sheath and DilatorNovember 13, 2020
K183174FlexCath Advance Steerable Sheath and DilatorNovember 26, 2018
K163268FlexCath Select Steerable Shealth and DilatorFebruary 2, 2017
K142684FlexCath Select Steerable Sheath (10 French)November 6, 2014
K123591FLEXCATH ADVANCE STEERABLE SHEATH (12 FRENCH)December 27, 2012
K102176FLEXCATH STEERABLE SHEATH (12 FRENCH), FLEXCATH STEERABLE SHEATH (10 FRENCH) MODEL 3FC12, 3FC10September 1, 2010