ClearanceBrief
510(k) K822130 ยท FZE Prosthesis, Nose, Internal

FRANCIS NASAL TUBE

ApplicantTekna Med Corp., Walker MI, US
DecisionSubstantially Equivalent, Oct 13, 1982
ReceivedJul 19, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K822130

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.