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FDA 510(k) Applications Submitted by ARISTA MEDI PRIMA
FDA 510(k) Number
Submission Date
Device Name
Applicant
K963742
09/17/1996
LATEX EXAMINATION GLOVES, POWDERED
ARISTA MEDI PRIMA
K970977
03/14/1997
LATEX EXAMINATION GLOVES, POWDER FREE
ARISTA MEDI PRIMA
K964629
11/19/1996
VINYL PATIENT EXAMINATION GLOVES
ARISTA MEDI PRIMA
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