ClearanceBrief
510(k) K812057 ยท FBK Endoscopic Injection Needle, Gastroenterology-Urology

VANCE CYSTOSCOPIC

ApplicantVance Products, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 31, 1981
ReceivedJul 21, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812057

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.