Access Bio Incorporate is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Access Bio Incorporate - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Access Bio Incorporate has 4 FDA 510(k) cleared medical devices. Based in North Brunswick, US.
Historical record: 4 cleared submissions from 2003 to 2005. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Access Bio Incorporate Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Access Bio Incorporate
4 devices
Cleared
Nov 29, 2005
CARESTART CARDIAC 3-IN-1 TROPONIN 1/CK-MB/MYOGLOBIN
Chemistry
134d
Cleared
Sep 05, 2003
CARESTART-PREGNANCY AND CARESTART PLUS-PREGNANCY
Chemistry
52d
Cleared
Jun 16, 2003
CARESTART HCG COMBO ONE-STEP PREGNANCY TEST AND CARESTART PLUS HCG COMBO...
Chemistry
75d
Cleared
Jun 13, 2003
CARESTART HCG ONE-STEP PREGNANCY TEST
Chemistry
72d