ClearanceBrief
510(k) K012864 ยท FCG Biopsy Needle

INTERJECT INJECTION THERAPY NEEDLE, MODELS 1810, 1811, 1815, 1816, 1820, 1821, 1825, 1826, 1830, 1831, 1835, 1836

ApplicantBoston Scientific Corp, Natick, MA, US
DecisionSubstantially Equivalent, Oct 24, 2001
ReceivedAug 27, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K012864

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.