ClearanceBrief
510(k) K982543 ยท DQX Wire, Guide, Catheter

SILVERSTREAK HYDROPHILIC GUIDEWIRE

ApplicantMicro Therapeutics, Inc., San Clemente CA, US
DecisionSubstantially Equivalent, Dec 11, 1998
ReceivedJul 21, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K982543

DateFirm and productCodeLinked 510(k)
Jun 7, 2007EV3 Neurovascular
Silver Speed Hydrophilic Guidewire, for placement of vascular catheters. Model # 103-0601-200.
Terminated
MKINone listed

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