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AMP PERITONEAL DIALYSIS PREP KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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