ClearanceBrief
510(k) K012624 ยท HRX Arthroscope

REPROCESSED ARTHROSCOPIC BLADES, ARTHROSCOPIC SHAVERS, SHAVER BLADE, BLADE, LIMITED REUSE BLADE, ARTHROSCOPIC BURS

ApplicantMedical Instruments Technology, Inc., St. George UT, US
DecisionSubstantially Equivalent, Nov 8, 2001
ReceivedAug 13, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K012624

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.