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PERITONEAL DIALYSIS KIT (ACUTE AND CHRONIC FORM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K874650
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1987
Days to Decision
26 days

PERITONEAL DIALYSIS KIT (ACUTE AND CHRONIC FORM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K874650
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1987
Days to Decision
26 days