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FDA 510(k) Applications Submitted by AMERICAN BANTEX CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K963218
08/16/1996
BANTEX SURGICAL LATEX GLOVES- TYPE 1 NATURAL RUBBER LATEX SURGICSL GLOVES, STERILE
AMERICAN BANTEX CORP.
K040754
03/24/2004
AMERICAN BANTEX MS 4 MINI SCOOTER
AMERICAN BANTEX CORP.
K031711
06/02/2003
TANGO, MODELS, BP1
AMERICAN BANTEX CORP.
K041963
07/21/2004
AMERICAN BANTEX HUMIDIFIER, DRY, BUBBLE, MODELS B9000, 3 PSI AND B9100, 6 PSI
AMERICAN BANTEX CORP.
K042104
08/04/2004
AMERICAN BANTEX, MODEL MS 3
AMERICAN BANTEX CORP.
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