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Renal Devices, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K810612HEMOPHRONApril 29, 1981
K801559HOLLO FIBER DIALYZEROctober 31, 1980
K802075HOLLOW FIBER DIALYZER HOLDERSeptember 16, 1980
K790696RDI-1 HOLLOW FIBER DIALYZERJune 20, 1979