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Izon Business Products, Inc.

FDA Regulatory Profile

Izon Business Products, 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 April 9, 2001.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K010328MULTIPLE (IZON DNA BLOOD COLLECTION KIT)April 9, 2001
K950257MULTIPLE (IZON DBS & URINE COLLECTION KIT)April 14, 1995
K950221MULTIPLE (IZON BLOOD & URINE COLLECTION KIT)March 21, 1995
K950246MULTIPLE (IZON URINE COLLECTION KIT)March 21, 1995

FDA data resources