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Laboratory Diagnostics Co., Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K801668 QUICK CEPTJHS1980-08-13 View
510(k) K761232 QUICK CULT SLIDE TEST FECAL OCCULT BLOODKHE1976-12-21 View
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