FDA 510(k) Applications Submitted by ALATECH HEALTHCARE, LLC.

FDA 510(k) Number Submission Date Device Name Applicant
K080606 03/04/2008 ALATECH POWDERED LATEX PATIENT EXAMINATION GLOVE ALATECH HEALTHCARE, LLC.
K082529 09/02/2008 ALATECH CHAMPION VYTEX LUBRICATED MALE LATEX CONDOM ALATECH HEALTHCARE, LLC.
K083761 12/18/2008 ALATECH POWDER FREE LATEX EXAMINATION GLOVE ALATECH HEALTHCARE, LLC.
K993887 11/16/1999 ALATECH LATEX CONDOM ALATECH HEALTHCARE, LLC.


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