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Innovacon, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K063673
INNOVACON FLIPCARD FECAL OCCULT BLOOD TEST DEVICE
March 5, 2007
K061718
INNOVACON SPECTRUM II TEST CARD
November 13, 2006
K062361
INNOVACON HCG UKTRA TEST DEVICE
October 23, 2006