ClearanceBrief
510(k) K831901 ยท HNL Probe, Lachrymal

LACIMAL INTUBATION SETS

ApplicantVisitec Co., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 12, 1983
ReceivedJun 14, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K831901

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.