ClearanceBrief
510(k) K881957 ยท KNW Instrument, Biopsy

HAWKINS-AKINS BLUNT NEEDLE ACCESS KIT

ApplicantN-S Medical Products, Gainesville FL, US
DecisionSubstantially Equivalent, May 20, 1988
ReceivedMay 10, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K881957

DateFirm and productCodeLinked 510(k)
Jul 13, 2010Medical Device Technologies, Inc.
Angiotech Access Needle. A) Hawkins Blunt Needle. STERILE. Product Number: 216057, 216107, 218057, 218107, 218157. 510k K881957. Qty Dist. - 3,220. B) Winged Guidewire Introducer Needle, Guid
Terminated
KNWNone listed

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