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FDA 510(k) Applications Submitted by AZOG, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K041748
06/29/2004
AZOG, INC. HCG ONE-STEP URINE HOME PREGNANCY TEST (DIP STICK, CASSETTE AND MIDSTREAM)
AZOG, INC.
K022680
08/12/2002
AZOG, INC. HCG ONE-STEP URINE PREGNANCY TEST STRIP (DIPSTICK)
AZOG, INC.
K022681
08/12/2002
AZOG, INC. HCG ONE-STEP URINE PREGNANCY TEST (DEVICE OR CASSETTE)
AZOG, INC.
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