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Keystone Diagnostics, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K875219 MODIFICATION TO KDI QUIK TEST MARIJUANA SCREENLDJ1988-06-24 View
510(k) K870197 KDI QUIK TEST(TM) MARIJUANA SCREENLDJ1987-06-01 View
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