ClearanceBrief
510(k) K822034 ยท DYG Catheter, Flow Directed

BALLOON WEDGE PRESSURE CATHETER

ApplicantZiehm International, Inc., Annapolis MD, US
DecisionSubstantially Equivalent, Aug 24, 1982
ReceivedJul 12, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K822034

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.