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Q-PORT SYSTEM KIT

Page Type
Cleared 510(K)
510(k) Number
K894650
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/1990
Days to Decision
231 days

Q-PORT SYSTEM KIT

Page Type
Cleared 510(K)
510(k) Number
K894650
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/1990
Days to Decision
231 days