ClearanceBrief
510(k) K833626 ยท GDY Gauze/Sponge, Internal, X-Ray Detectable

FLORET FOAM PREP SPONGE

ApplicantRitmed, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 17, 1984
ReceivedOct 14, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K833626

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.