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Scandimed. A.S.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K031238VARICES NEEDLEOctober 4, 2004
K031236AUTO-BAND LIGATORNovember 14, 2003