ClearanceBrief
510(k) K083769 ยท HHW Pessary, Vaginal

MODIFICATION TO URESTA PESSARY

ApplicantEastmed, Inc., Dundas, CA
DecisionSubstantially Equivalent, Jan 14, 2009
ReceivedDec 18, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K083769

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.