ClearanceBrief
510(k) K010708 ยท FMF Syringe, Piston

APPLICATOR TIP/DUAL SPRAYER KIT

ApplicantInterpore Cross Intl., Irvine CA, US
DecisionSubstantially Equivalent, Apr 30, 2001
ReceivedMar 9, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K010708

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.