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Selicor, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K030382
SELITHERM, MODEL C100
April 1, 2003
K020227
SELICOR, MODELS A100 & D100
July 30, 2002