ClearanceBrief
510(k) K972922 ยท EMX Balloon, Epistaxis

VYKER SILICONE EPISTAXIS CATHETER V-27030, VYKER SILICONE EPISTAXIS CATHETER KIT V-2703K

ApplicantInterview Medical Technology Corp., El Dorado Hills CA, US
DecisionSubstantially Equivalent, Oct 8, 1997
ReceivedAug 8, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K972922

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.