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DUAL LUMEN NEEDLE (PRODUCT CHANGE)

Page Type
Cleared 510(K)
510(k) Number
K860515
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1986
Days to Decision
21 days

DUAL LUMEN NEEDLE (PRODUCT CHANGE)

Page Type
Cleared 510(K)
510(k) Number
K860515
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1986
Days to Decision
21 days