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FDA 510(k) Applications Submitted by UNOTECH DIAGNOSTICS, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K971886
05/22/1997
ACCUTEST HCG-URINE
UNOTECH DIAGNOSTICS, INC.
K981838
05/26/1998
ACCUSTRIP HCG-URINE MODEL NUMBER HCG-002
UNOTECH DIAGNOSTICS, INC.
K032987
09/24/2003
ACCUTEST HCG-COMBO MODEL,HCG-004, ACCUSTRIP HCG-COMBO MODEL, HCG-005
UNOTECH DIAGNOSTICS, INC.
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