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ACUTE PERITONEAL DIALYSIS KIT

Page Type
Cleared 510(K)
510(k) Number
K870472
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/1987
Days to Decision
22 days

ACUTE PERITONEAL DIALYSIS KIT

Page Type
Cleared 510(K)
510(k) Number
K870472
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/1987
Days to Decision
22 days