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Dws, 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
K231142
Temporis, Irix Plus
April 25, 2024
K761050
HEPARIN PUMP
December 30, 1976
K761051
BI-FLOW NEEDLE
December 30, 1976