Last synced on 25 January 2026 at 3:41 am

Dimesol Disposable AV Fistula Needle Set (Non-Safety Series) and Dimesol Disposable AV Fistula Needle Set (Safety Series)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171505
510(k) Type
Traditional
Applicant
Dimesol, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/2018
Days to Decision
359 days
Submission Type
Summary

Dimesol Disposable AV Fistula Needle Set (Non-Safety Series) and Dimesol Disposable AV Fistula Needle Set (Safety Series)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171505
510(k) Type
Traditional
Applicant
Dimesol, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/2018
Days to Decision
359 days
Submission Type
Summary