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Quinton Electrophysiology Corp.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K971570 EPXPRESS SYSTEM (TIMBERWOLF REVISION) /000391DRR1997-12-29 View
510(k) K925346 EP AMP, MODEL #901DRR1993-04-30 View
510(k) K893836 EPLAB (ELECTROCARDIOGRAPHIC MONITOR)DSH1989-09-08 View
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