Azog, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Azog, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Azog, Inc. has 3 FDA 510(k) cleared medical devices. Based in Phillipsburg, US.
Historical record: 3 cleared submissions from 2002 to 2004. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Azog, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Azog, Inc.
3 devices
Cleared
Aug 09, 2004
AZOG, INC. HCG ONE-STEP URINE HOME PREGNANCY TEST (DIP STICK, CASSETTE AND...
Chemistry
41d
Cleared
Nov 01, 2002
AZOG, INC. HCG ONE-STEP URINE PREGNANCY TEST STRIP (DIPSTICK)
Chemistry
81d
Cleared
Nov 01, 2002
AZOG, INC. HCG ONE-STEP URINE PREGNANCY TEST (DEVICE OR CASSETTE)
Chemistry
81d