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DISPOSABLE PERITONEAL DIALYSIS EXTENSION

Page Type
Cleared 510(K)
510(k) Number
K791722
510(k) Type
Traditional
Applicant
AMERICAN MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1979
Days to Decision
78 days

DISPOSABLE PERITONEAL DIALYSIS EXTENSION

Page Type
Cleared 510(K)
510(k) Number
K791722
510(k) Type
Traditional
Applicant
AMERICAN MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1979
Days to Decision
78 days