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Immuno-Diagnostic Products, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K854207EBV(EPSTEIN-BARR VIRUS) TEST KITApril 24, 1986
K811021HERPESNovember 5, 1981
K811562TOXOPLASMOSIS TEST KITJuly 16, 1981
K811022ANA TEST KITApril 23, 1981
K801959FTA-ABS TESTOctober 23, 1980
K801963CMV TEST KITOctober 23, 1980
K801960ANTI-DS/N-DNA TEST KITOctober 10, 1980
K801961RF-II TEST KITOctober 10, 1980