ClearanceBrief
510(k) K981554 ยท HNO Keratome, Ac-Powered

MICRATOME MS7000 -ADVANCED CORNEAL/REFRACTIVE INSTRUMENTATION (ACRI)

ApplicantMicra Instruments , Ltd., Luton, Bedfordshire, GB
DecisionSubstantially Equivalent, Dec 22, 1998
ReceivedMay 1, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K981554

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.