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/ Cyberex Corp.
Cyberex Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K810837
CYBER 80 HEMODIALYZER
May 5, 1981
K802478
CYBER 120 HEMODIALYZER
March 20, 1981
K801377
CYBER 120 HEMODIALYZER
August 27, 1980
K790824
REPGREEN ULTRAFILTRATION MONITOR
June 27, 1979