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Prodesse, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K091053PROPARAFLU+ASSAYNovember 20, 2009
K092500MODIFICATION TO PROFLU+ ASSAYAugust 20, 2009
K090239PROGASTRO CD ASSAYApril 16, 2009
K082688PRO HMPV+ ASSAYNovember 7, 2008
K081030MODIFICATION TO PROFLU+ ASSAYMay 2, 2008
K073029PROFLU+ ASSAYJanuary 4, 2008