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ULTRX(TM) 850 ARTIFICIAL KIDNEY

Page Type
Cleared 510(K)
510(k) Number
K884353
510(k) Type
Traditional
Applicant
CD MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/1988
Days to Decision
52 days

ULTRX(TM) 850 ARTIFICIAL KIDNEY

Page Type
Cleared 510(K)
510(k) Number
K884353
510(k) Type
Traditional
Applicant
CD MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/1988
Days to Decision
52 days