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Halkey-Roberts Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K061143
ROBERTSITE STOPCOCK
May 10, 2006
K040634
ROBERTSITE VIAL ADAPTER, MODEL 245700021
March 23, 2004