ClearanceBrief
510(k) K880209 ยท EIL Gauge, Depth, Instrument, Dental

PERIODONTAL PROBE - AUTOPROBE

ApplicantDentsply Intl., York PA, US
DecisionSubstantially Equivalent, Apr 27, 1988
ReceivedJan 15, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880209

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.