ClearanceBrief
510(k) K992687 ยท HMY Keratome, Battery-Powered

MILLENIUM MICROKERATOME, MODEL IMD-001

ApplicantIndustrial & Medical Design, Inc., Los Angeles CA, US
DecisionSubstantially Equivalent, Sep 24, 1999
ReceivedAug 10, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K992687

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.