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Percudisc, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K920673 PERCUDISC PLDD DELIVERY SYSTEM/PROCEDURE KITGEX1992-08-13 View
510(k) K910823 PERCUDISC(TM) SYSTEMGEX1991-12-30 View
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