ClearanceBrief
510(k) K133682 ยท HRX Arthroscope

SCHOELLY ARTHROSCOPE

ApplicantScholly Fiberoptic GmbH, Ayer MA, US
DecisionSubstantially Equivalent, Jun 2, 2014
ReceivedDec 2, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K133682

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.