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QUINTON SINGLE LUMEN CATHETER

Page Type
Cleared 510(K)
510(k) Number
K893188
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/1989
Days to Decision
34 days

QUINTON SINGLE LUMEN CATHETER

Page Type
Cleared 510(K)
510(k) Number
K893188
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/1989
Days to Decision
34 days