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Disco, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K923085 QUICKLAMP SYSTEMDXC1993-02-12 View
510(k) K914149 FEMORAL ARTERY PRESSURE PAD/DISKDXC1991-12-13 View
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