ClearanceBrief
510(k) K173321 · BSP Needle, Conduction, Anesthetic (W/Wo Introducer)

StimuQuik 21G x 9cm (3.5”) Peripheral Nerve Block Needle, StimuQuik Echo 21G x 9cm (3.5”) Peripheral Nerve Block Needle, StimuQuik 21G x 15cm (6”) Peripheral Nerve Block Needle, StimuQuik Echo 21G x 15cm (6”) Peripheral Nerve Block Needle, StimuQuik 21G x 2.5cm (1”) Peripheral Nerve Block Needle

ApplicantTeleflex Medical, Morrisville NC, US
DecisionSubstantially Equivalent, Apr 25, 2018
ReceivedOct 20, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K173321

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.