ClearanceBrief
510(k) K191594 ยท HRX Arthroscope

Nuvis Battery Arthroscope

ApplicantIntegrated Endoscopy, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Jul 11, 2019
ReceivedJun 17, 2019
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K191594

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.