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GESCO PER-Q-CATH NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K911215
510(k) Type
Traditional
Applicant
GESCO INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/1991
Days to Decision
79 days

GESCO PER-Q-CATH NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K911215
510(k) Type
Traditional
Applicant
GESCO INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/1991
Days to Decision
79 days