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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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