ClearanceBrief
Company ยท US

Medtronic Cryocath, LP

FDA 510(k) clearances and medical device recalls filed under this name, 2010 to 2020. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DRACatheter, Steerable4
DYBIntroducer, Catheter2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 13, 2020K202620FlexCath Advance Steerable Sheath and Dilator
Medtronic Cryocath, LP
DRA
Nov 26, 2018K183174FlexCath Advance Steerable Sheath and Dilator
Medtronic Cryocath, LP
DRA
Feb 2, 2017K163268FlexCath Select Steerable Shealth and Dilator
Medtronic Cryocath, LP
DYB
Nov 6, 2014K142684FlexCath Select Steerable Sheath (10 French)
Medtronic Cryocath, LP
DYB
Dec 27, 2012K123591FLEXCATH ADVANCE STEERABLE SHEATH (12 FRENCH)
Medtronic Cryocath, LP
DRA
Sep 1, 2010K102176FLEXCATH STEERABLE SHEATH (12 FRENCH), FLEXCATH STEERABLE SHEATH (10 FRENCH) MODEL 3FC12, 3FC10
Medtronic Cryocath, LP, CA
DRA

Latest recalls

DateFirm and productCodeLinked 510(k)
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