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Hager Worldwide, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K061933
HAGER MIRAMATIC BOX SHARPS CONTAINER AND CAP TRAP NEEDLE RE-CAPPER
November 16, 2006
K043322
MIRAMATIC SAFE SYRINGE SYSTEM
July 21, 2005
K050658
RESO-PAC PERIODONTAL DRESSING
May 27, 2005