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AMP PERITONEAL DIALYSIS PREP KIT

Page Type
Cleared 510(K)
510(k) Number
K810840
510(k) Type
Traditional
Applicant
AMERICAN MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1981
Days to Decision
33 days

AMP PERITONEAL DIALYSIS PREP KIT

Page Type
Cleared 510(K)
510(k) Number
K810840
510(k) Type
Traditional
Applicant
AMERICAN MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1981
Days to Decision
33 days