American Bantex Corp.

American Bantex Corp. holds 5 FDA 510(k) medical device clearances, first cleared 1996, most recent 2004.

Top product codes for American Bantex Corp.

Recent clearances by American Bantex Corp.

K042104 — AMERICAN BANTEX, MODEL MS 3Code INI·2004-10-21
K041963 — AMERICAN BANTEX HUMIDIFIER, DRY, BUBBLE, MODELS B9000, 3 PSI AND B9100, 6 PSICode BTT·2004-10-20
K040754 — AMERICAN BANTEX MS 4 MINI SCOOTERCode INI·2004-07-23
K031711 — TANGO, MODELS, BP1Code ITI·2003-12-18
K963218 — BANTEX SURGICAL LATEX GLOVES- TYPE 1 NATURAL RUBBER LATEX SURGICSL GLOVES, STERILECode KGO·1996-10-30

Data sourced from openFDA. This site is unofficial and independent of the FDA.