ClearanceBrief
510(k) K890493 ยท EIL Gauge, Depth, Instrument, Dental

FLORIDA PROBE PERIODONTAL PROBE

ApplicantFlorida Probe Corp., Gainesville FL, US
DecisionSubstantially Equivalent, Mar 13, 1989
ReceivedJan 31, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K890493

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.