ClearanceBrief
510(k) K980717 ยท KNA Instrument, Manual, Specialized Obstetric-Gynecologic

UROMED SLING KIT

ApplicantUromed Corp., Needham MA, US
DecisionSubstantially Equivalent, May 22, 1998
ReceivedFeb 24, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K980717

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.