ClearanceBrief
510(k) K905461 ยท EKS File, Pulp Canal, Endodontic

PROCEDURE KIT/ROUTINE DENTAL PROCEDURES

ApplicantAngiosystems, Inc., Great Neck NY, US
DecisionUnknown, Mar 5, 1991
ReceivedDec 5, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K905461

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.