American Bantex Corp. is one of 24987 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Bantex Corp. - FDA 510(k) Cleared Devices
Recent clearances: AMERICAN BANTEX, MODEL MS 3, AMERICAN BANTEX HUMIDIFIER, DRY, BUBBLE, MODELS B9000, 3 PSI AND B9100, 6 PSI, AMERICAN BANTEX MS 4 MINI SCOOTER
5
Total
5
Cleared
0
Denied
American Bantex Corp. has 5 FDA 510(k) cleared medical devices. Based in Bountiful, US.
Historical record: 5 cleared submissions from 1996 to 2004. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by American Bantex Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Bantex Corp.
5 devices
Cleared
Oct 21, 2004
AMERICAN BANTEX, MODEL MS 3
Physical Medicine
78d
Cleared
Oct 20, 2004
AMERICAN BANTEX HUMIDIFIER, DRY, BUBBLE, MODELS B9000, 3 PSI AND B9100, 6 PSI
Anesthesiology
91d
Cleared
Jul 23, 2004
AMERICAN BANTEX MS 4 MINI SCOOTER
Physical Medicine
121d
Cleared
Dec 18, 2003
TANGO, MODELS, BP1
Physical Medicine
199d
Cleared
Oct 30, 1996
BANTEX SURGICAL LATEX GLOVES- TYPE 1 NATURAL RUBBER LATEX SURGICSL GLOVES,...
General Hospital
75d