ClearanceBrief
510(k) K813286 ยท GDY Gauze/Sponge, Internal, X-Ray Detectable

PRE-PACK TENS

ApplicantCunningham Woodland, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 22, 1982
ReceivedNov 23, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K813286

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.