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Vitajet 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
K962625
VITAJET
December 10, 1996
K945548
MEDIVAX
November 20, 1995
K924447
VITAPEN
September 27, 1993