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INJECTOR NEEDLE/SNARE

Page Type
Cleared 510(K)
510(k) Number
K040961
510(k) Type
Traditional
Applicant
UNITED STATES ENDOSCOPY GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/2004
Days to Decision
86 days
Submission Type
Statement

INJECTOR NEEDLE/SNARE

Page Type
Cleared 510(K)
510(k) Number
K040961
510(k) Type
Traditional
Applicant
UNITED STATES ENDOSCOPY GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/2004
Days to Decision
86 days
Submission Type
Statement