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PERITONEAL CATHETERS WITH AN ADDED FUNCTION

Page Type
Cleared 510(K)
510(k) Number
K890288
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1989
Days to Decision
67 days

PERITONEAL CATHETERS WITH AN ADDED FUNCTION

Page Type
Cleared 510(K)
510(k) Number
K890288
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1989
Days to Decision
67 days