Last synced on 25 January 2026 at 3:41 am

EndoVive Initial Placement Standard PEG Kit with ENFit Connector, EndoVive Initial Placement Safety PEG Kit with ENFit Connector

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150679
510(k) Type
Traditional
Applicant
Boston Scientific Corp
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
5/29/2015
Days to Decision
73 days
Submission Type
Summary

EndoVive Initial Placement Standard PEG Kit with ENFit Connector, EndoVive Initial Placement Safety PEG Kit with ENFit Connector

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150679
510(k) Type
Traditional
Applicant
Boston Scientific Corp
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
5/29/2015
Days to Decision
73 days
Submission Type
Summary