ClearanceBrief
510(k) K880322 ยท KMH Sterilizer, Dry Heat

DENTRONIX DDS 5000 DRY HEAT STERILIZATION SYSTEM

ApplicantDentronix, Inc., Ivyland PA, US
DecisionSubstantially Equivalent, Jul 13, 1988
ReceivedJan 27, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880322

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.