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Dianon Systems, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K882105 CODE #D2020-FINE NEEDLE ASPIRATION BIOPSY SYSTEMGAA1988-07-11 View
510(k) K872597 FINE NEEDLE ASPIRATION BIOPSY SYSTEM-PROSTATEDWO1987-07-28 View
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