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INJECTION NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K132065
510(k) Type
Traditional
Applicant
ENDOCHOICE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2014
Days to Decision
198 days
Submission Type
Summary

INJECTION NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K132065
510(k) Type
Traditional
Applicant
ENDOCHOICE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2014
Days to Decision
198 days
Submission Type
Summary