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CATHETER FINGER GRIP

Page Type
Cleared 510(K)
510(k) Number
K771483
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/1977
Days to Decision
116 days

CATHETER FINGER GRIP

Page Type
Cleared 510(K)
510(k) Number
K771483
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/1977
Days to Decision
116 days