ClearanceBrief
510(k) K983181 ยท HHI System, Abortion, Vacuum

CYTOPREP

ApplicantCytoprep Inc. Est., Eschen, LI
DecisionSubstantially Equivalent, Nov 16, 1998
ReceivedSep 11, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K983181

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.