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Horizon Medical, 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
K980171
DERMASENSE PLUS DISPERSIVE ELECTRODE
February 27, 1998
K944969
STERI-LUB LUBRICATION GEL
February 27, 1995
K883576
HORIZON ORTHOPEDIC PIN PROTECTOR
September 30, 1988