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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