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DUAL LUMEN NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K833308
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/1983
Days to Decision
92 days

DUAL LUMEN NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K833308
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/1983
Days to Decision
92 days