Last synced on 25 January 2026 at 3:41 am

SafeSept Transseptal Guidewire

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170671
510(k) Type
Traditional
Applicant
Pressure Products Medical Device Manufacturing, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/2017
Days to Decision
228 days
Submission Type
Summary

SafeSept Transseptal Guidewire

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170671
510(k) Type
Traditional
Applicant
Pressure Products Medical Device Manufacturing, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/2017
Days to Decision
228 days
Submission Type
Summary