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QUINTON CATHETER FINGER GRIP

Page Type
Cleared 510(K)
510(k) Number
K811266
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/1981
Days to Decision
37 days

QUINTON CATHETER FINGER GRIP

Page Type
Cleared 510(K)
510(k) Number
K811266
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/1981
Days to Decision
37 days