ClearanceBrief
510(k) K090261 ยท BSP Needle, Conduction, Anesthetic (W/Wo Introducer)

PORTEX TUOHY EPIDURAL NEEDLE 17G, PORTEX TUOHY EPIDURAL NEEDLE 18G

ApplicantSmiths Medical Asd, Inc., Keene NH, US
DecisionSubstantially Equivalent, May 1, 2009
ReceivedFeb 3, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K090261

No recall in the FDA data names this 510(k).

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