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NEEDLE CANNULA

Page Type
Cleared 510(K)
510(k) Number
K911494
510(k) Type
Traditional
Applicant
UNITED STATES ENDOSCOPY GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/1991
Days to Decision
89 days

NEEDLE CANNULA

Page Type
Cleared 510(K)
510(k) Number
K911494
510(k) Type
Traditional
Applicant
UNITED STATES ENDOSCOPY GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/1991
Days to Decision
89 days