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ULTRAMAX III, DIALYZER REPROCESSING DEVICE

Page Type
Cleared 510(K)
510(k) Number
K860026
510(k) Type
Traditional
Applicant
MEDICORP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/1986
Days to Decision
70 days

ULTRAMAX III, DIALYZER REPROCESSING DEVICE

Page Type
Cleared 510(K)
510(k) Number
K860026
510(k) Type
Traditional
Applicant
MEDICORP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/1986
Days to Decision
70 days