ClearanceBrief
510(k) K925083 ยท HRX Arthroscope

ENDOTRAK SYSTEM

ApplicantInstratek, Inc., Houston TX, US
DecisionSubstantially Equivalent, Apr 27, 1993
ReceivedOct 7, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K925083

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.