ClearanceBrief
510(k) K122905 ยท HQB Photocoagulator And Accessories

PEREGRINE 23GA CURVED LASER PROBE

ApplicantPeregrine Surgical , Ltd., New Britain PA, US
DecisionSubstantially Equivalent, Apr 30, 2013
ReceivedSep 21, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K122905

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.