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ER-REBOA Catheter

Page Type
Cleared 510(K)
510(k) Number
K172790
510(k) Type
Traditional
Applicant
Prytime Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2017
Days to Decision
54 days
Submission Type
Summary

ER-REBOA Catheter

Page Type
Cleared 510(K)
510(k) Number
K172790
510(k) Type
Traditional
Applicant
Prytime Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2017
Days to Decision
54 days
Submission Type
Summary