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SafeSept® Transseptal Guidewire (SS-140)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221707
510(k) Type
Special
Applicant
Pressure Products Medical Device Manufacturing LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2022
Days to Decision
93 days
Submission Type
Summary

SafeSept® Transseptal Guidewire (SS-140)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221707
510(k) Type
Special
Applicant
Pressure Products Medical Device Manufacturing LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2022
Days to Decision
93 days
Submission Type
Summary