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Ekom S.R.O.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K091871DK50 DSOctober 23, 2009
K060781MEDICAL COMPRESSOR, MODELS DK50 D AND DMOctober 3, 2006