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Kantron Cardiovascular, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K812586 KANTRON 504 HEARTSTATIONLDD1981-12-29 View
510(k) K812587 MONO 2 OXYGEN MONITORCCL1981-10-06 View
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