ClearanceBrief
510(k) K991946 ยท EIA Unit, Operative Dental

ULTRA-KLEEN POWDER FOR DENTAL UNIT WATER LINES, MODELS 513P, 505L

ApplicantSterilex Corp., Owins Mills MD, US
DecisionSubstantially Equivalent, Sep 3, 1999
ReceivedJun 9, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K991946

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.