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Rejoni Intrauterine Catheter

Page Type
Cleared 510(K)
510(k) Number
K222798
510(k) Type
Traditional
Applicant
Rejoni, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2022
Days to Decision
91 days
Submission Type
Summary

Rejoni Intrauterine Catheter

Page Type
Cleared 510(K)
510(k) Number
K222798
510(k) Type
Traditional
Applicant
Rejoni, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2022
Days to Decision
91 days
Submission Type
Summary