ClearanceBrief
510(k) K043580 ยท DQY Catheter, Percutaneous

ALLIGATOR RETRIEVAL DEVICE (ARD)

ApplicantChestnut Medical Technologies, Inc., Palo Alto CA, US
DecisionSubstantially Equivalent, Mar 24, 2005
ReceivedDec 28, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K043580

DateFirm and productCodeLinked 510(k)
Apr 16, 2014Micro Therapeutics Inc, Dba Ev3 Neurovascular
Alligator Retrieval Device (ARD). Used in the peripheral and neurovasculature for foreign body removal.
Terminated
DQYNone listed

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