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Sapimed S.P.A.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K070881LEM HEMORRHOIDAL LIGATOR, MODELS A.5650, A.5660September 26, 2007
K070913SELF-LIGHT DISPOSABLE ANOSCOPEAugust 10, 2007
K070915SAPIMED DISPOSABLE SIGMOIDOSCOPEJuly 6, 2007