ClearanceBrief
510(k) K850312 ยท HHI System, Abortion, Vacuum

GYNASPYR VACUUM CURETTAGE UNIT

ApplicantRoseburg SA, Washington DC, US
DecisionSubstantially Equivalent, Feb 28, 1985
ReceivedJan 25, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K850312

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.