ClearanceBrief
510(k) K961524 ยท HNY Cystotome

STERILAB CANNULAS, STERILAB CYSTOTMES, STERILAB NEEDLES AND STERILAB LENS MANIPULATORS

ApplicantSterilab, Inc., Carlsbad CA, US
DecisionSubstantially Equivalent, May 16, 1996
ReceivedApr 22, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K961524

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.