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Amtec Diagnostics International, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K882998 ACUTE PHASE C-REACTIVE PROTEIN LATEX AGGLU. TESTDCK1988-09-07 View
510(k) K873064 AMTEC RHEUMATOID FACTOR LATEX AGGLUTINATION KITDHR1987-11-04 View
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