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Axiom, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K883887
AXIOM ATRAUM WOUND DRAINS
February 17, 1989
K842443
AXIOM STABLE II TRIGLYCERIDES TEST
September 13, 1984
K842442
AXIOM STABLE II URIC ACID TEST
August 16, 1984
K842441
AXIOM STABLE II CHOLESTEROL TEST
July 25, 1984