ClearanceBrief
510(k) K823220 ยท DPS Electrocardiograph

COSMOS

ApplicantNihon Kohden America, Inc., Foothill CA, US
DecisionSubstantially Equivalent, Nov 24, 1982
ReceivedNov 1, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823220

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.