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Ilex Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K860639
IONIZED CALCIUM AND BLOOD PH TESTCARDS
April 21, 1986
K860543
BLOOD UREA NITROGEN (BUN) TESTCARD
April 21, 1986
K853068
ILEX PROMPT CLINICAL CHEMISTRY ANALYER
October 31, 1985