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Axiom, Inc.

FDA Regulatory Profile

Axiom, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 17, 1989.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K883887AXIOM ATRAUM WOUND DRAINSFebruary 17, 1989
K842443AXIOM STABLE II TRIGLYCERIDES TESTSeptember 13, 1984
K842442AXIOM STABLE II URIC ACID TESTAugust 16, 1984
K842441AXIOM STABLE II CHOLESTEROL TESTJuly 25, 1984

FDA data resources