Althin Medical AB

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K992563A-22 HEMODIALYZERJanuary 18, 2000
K992573AF-220 HEMODIALYZERJanuary 18, 2000
K992564AF-180 HEMODIALYZERJanuary 18, 2000
K992566AF-150 HEMODIALYZERJanuary 18, 2000
K992594A-15 HEMODIALYZERSeptember 24, 1999
K992565A-18 HEMODIALYZERSeptember 23, 1999
K990010ALTHIN MEDICAL AB ALTRACART IIApril 15, 1999