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Dobre, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K924891 PLEXUS PULSER I, PLEXUS PULSER IIJOW1993-06-07 View
510(k) K770521 ELECTROCARDIOGRAPHIC ELECTRODES, DISP.DRX1977-03-29 View
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