ClearanceBrief
510(k) K841275 ยท DRM Compressor, Cardiac, External

FINE NEEDLE ASPIRATION DEVICE

ApplicantGyneco, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 17, 1984
ReceivedMar 27, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K841275

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.