ClearanceBrief
510(k) K010098 ยท FGM Probe And Director, Gastro-Urology

MODIFICATION TO CAVERMAP SURGICAL AID

ApplicantUromed Corp., Norwood MA, US
DecisionSubstantially Equivalent, Feb 1, 2001
ReceivedJan 11, 2001
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K010098

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.