ClearanceBrief
510(k) K152699 ยท GWG Endoscope, Neurological

Apollo System

ApplicantPenumbra, Inc., Alameda CA, US
DecisionSubstantially Equivalent, Mar 17, 2016
ReceivedSep 21, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K152699

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.