ClearanceBrief
510(k) K052791 ยท DQY Catheter, Percutaneous

MODIFICATION TO: AMPHIRION DEEP 0.014 OTW PTA BALLOON CATHETER

ApplicantInvatec Innovative Technologies, S.R.L., Plymouth MN, US
DecisionSubstantially Equivalent, Nov 4, 2005
ReceivedOct 3, 2005
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K052791

DateFirm and productCodeLinked 510(k)
Nov 6, 2015Medtronic Vascular, Inc.
Amphirion Deep OTW PTA Balloon Catheter: Model numbers: US: AMP015020152 AMP020150152 AMP025120152 AMP030080152 AMP040040152 AMP225210152 AMP020040152 AMP025040152 AMP025150152 AMP030120152 AMP040080
Terminated
DQYNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.