ClearanceBrief
510(k) K133234 ยท HKY Tonometer, Manual

T-TYPE D-KAT, R-TYPE D-KAT

ApplicantKeeler Limited, Broomall PA, US
DecisionSubstantially Equivalent, Feb 21, 2014
ReceivedOct 21, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K133234

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.