ClearanceBrief
510(k) K820226 ยท HTW Bit, Drill

UNIVERSALL DRILL GUIDE

ApplicantOrtho Pared Instruments, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 4, 1982
ReceivedJan 27, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820226

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.