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Estracorporeal, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K915130MAT MEMBRANE AUTOTRANSFUSION SYSTEMFebruary 22, 1993
K790382COIL DIALYSIS, MODELS DM-360 AND DM-360-May 2, 1979