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Clonetics Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K890701
ENDOTHELIAL GROWTH MEDIUM (EGM)
February 24, 1989
K890700
MELANOCYTE GROWTH MEDIUM (MGM)
February 24, 1989
K880999
EPIPACK
March 24, 1988
K881000
KERATINOCYTE GROWTH MEDIUM (KGM)
March 21, 1988