ClearanceBrief
510(k) K905014 ยท HRX Arthroscope

AMSET PLD SYSTEM

ApplicantAdvanced Med/Surg, Inc., Hayward CA, US
DecisionSubstantially Equivalent, Apr 1, 1991
ReceivedNov 6, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K905014

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.