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PERITONEAL DIALYSIS CYCLER SET

Page Type
Cleared 510(K)
510(k) Number
K813069
510(k) Type
Traditional
Applicant
AMERICAN MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1981
Days to Decision
17 days

PERITONEAL DIALYSIS CYCLER SET

Page Type
Cleared 510(K)
510(k) Number
K813069
510(k) Type
Traditional
Applicant
AMERICAN MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1981
Days to Decision
17 days