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Promedon S.A
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K110420
OPHIRA MINI SLING SYSTEM
May 8, 2012
K033691
SAFYRE VS AND SAFYRE T
December 19, 2003
K020007
SAFYRE SLING SYSTEM
March 21, 2002