ClearanceBrief
510(k) K051905 ยท FBK Endoscopic Injection Needle, Gastroenterology-Urology

UROPLASTY RIGID ENDOSCOPIC NEEDLE

ApplicantUroplasty, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Aug 29, 2005
ReceivedJul 14, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K051905

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.