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Inmed Ltda.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K030081CSF400 AND CSF600October 6, 2003
K030887LEKTROGEL, MODEL LK3001June 13, 2003
K030889ULTRAEKOGEL MODELS EK 2000 & EK 2001May 23, 2003