ClearanceBrief
510(k) K812011 ยท HOE Caliper, Ophthalmic

BLADE GAUGE

ApplicantKoi, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 28, 1981
ReceivedJul 17, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812011

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.