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Interject Injection Therapy Needle Catheter

Page Type
Cleared 510(K)
510(k) Number
K171454
510(k) Type
Traditional
Applicant
Boston Scientific Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/2017
Days to Decision
51 days
Submission Type
Summary

Interject Injection Therapy Needle Catheter

Page Type
Cleared 510(K)
510(k) Number
K171454
510(k) Type
Traditional
Applicant
Boston Scientific Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/2017
Days to Decision
51 days
Submission Type
Summary