Izon Business Products, Inc.

FDA Regulatory Profile

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
K950246MULTIPLE (IZON URINE COLLECTION KIT)March 21, 1995
K950221MULTIPLE (IZON BLOOD & URINE COLLECTION KIT)March 21, 1995