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pREBOA-PRO Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243795
510(k) Type
Traditional
Applicant
Prytime Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/2025
Days to Decision
269 days
Submission Type
Summary

pREBOA-PRO Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243795
510(k) Type
Traditional
Applicant
Prytime Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/2025
Days to Decision
269 days
Submission Type
Summary