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Arch Development Group

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K913047 STERILESERT(TM) CABLE AND POLE DRAPEKKX1991-10-02 View
510(k) K912765 STASIS BUTTON PRSSURE DEVICEMHW1991-08-12 View
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