ClearanceBrief
510(k) K960519 ยท FBK Endoscopic Injection Needle, Gastroenterology-Urology

MARTECH ENDOSCOPIC INJECTION NEEDLE

ApplicantMartech Medical Products, Inc., Harleysville PA, US
DecisionSubstantially Equivalent, May 1, 1996
ReceivedFeb 5, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960519

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.