ClearanceBrief
510(k) K943370 ยท EJI Syringe, Cartridge

IMPULSE SEALER PRODUCT LINE

ApplicantUltradent Products, Inc., South Jordan UT, US
DecisionSubstantially Equivalent, Oct 21, 1994
ReceivedJul 13, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K943370

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.