ClearanceBrief
510(k) K863725 ยท HNN Knife, Ophthalmic

CATARACT DIAMOND KNIFE

ApplicantMedical Technology Development Corp., Clearwater FL, US
DecisionSubstantially Equivalent, Oct 31, 1986
ReceivedSep 23, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K863725

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.