ClearanceBrief
510(k) K943635 ยท HAE Rongeur, Manual

ULTRA-LINE RONGEUR

ApplicantV. Mueller Neuro/Spine, San Carlos CA, US
DecisionSubstantially Equivalent, Dec 7, 1994
ReceivedJul 27, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K943635

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.