Last synced on 30 May 2025 at 11:05 pm

NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250592
510(k) Type
Traditional
Applicant
Northeast Scientific, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/2025
Days to Decision
74 days
Submission Type
Summary

NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250592
510(k) Type
Traditional
Applicant
Northeast Scientific, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/2025
Days to Decision
74 days
Submission Type
Summary