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REPAIR KIT QUINTON TRIPLE LUMEN RIGHT ATRIAL CATHE

Page Type
Cleared 510(K)
510(k) Number
K853860
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1985
Days to Decision
31 days

REPAIR KIT QUINTON TRIPLE LUMEN RIGHT ATRIAL CATHE

Page Type
Cleared 510(K)
510(k) Number
K853860
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1985
Days to Decision
31 days