Med2000 S.R.L.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K041974MED2000 NEBULIZER COMPRESSOR, MODELS P3, P4, P5 WITH NEBULIZERAugust 24, 2004
K041327MED2000 SPA NEBULIZER ANDYFLOW, MODEL A1/C WITH ACCESSORIESJuly 20, 2004
K031908MED2000 SPA NEBULIZER COMPRESSORS, MODELS P1 AND P2, WITH NEBULIZER, AND MED2000 SPA NEBULIZER, MODEJanuary 14, 2004