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MODIFIED QUINTON SINGLE LUMEN CATHETER

Page Type
Cleared 510(K)
510(k) Number
K896252
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/1990
Days to Decision
91 days

MODIFIED QUINTON SINGLE LUMEN CATHETER

Page Type
Cleared 510(K)
510(k) Number
K896252
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/1990
Days to Decision
91 days