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Hersill, S.L.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
2
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K094003
REVIVATOR
September 17, 2010
K093241
V7 PORTABLE SUCTION UNITS
April 27, 2010