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Sie-Med, 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
K003130
REGUTHERM 952 THERMOGRAPHIC SYSTEM
February 16, 2001
K964083
ULTRATHERM (908)
April 3, 1997