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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact