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pREBOA-PRO Catheter

Page Type
Cleared 510(K)
510(k) Number
K200459
510(k) Type
Traditional
Applicant
Prytime Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2020
Days to Decision
99 days
Submission Type
Summary

pREBOA-PRO Catheter

Page Type
Cleared 510(K)
510(k) Number
K200459
510(k) Type
Traditional
Applicant
Prytime Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2020
Days to Decision
99 days
Submission Type
Summary