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RenovoCath

Page Type
Cleared 510(K)
510(k) Number
K160067
510(k) Type
Traditional
Applicant
RenovoRx, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2017
Days to Decision
419 days
Submission Type
Summary

RenovoCath

Page Type
Cleared 510(K)
510(k) Number
K160067
510(k) Type
Traditional
Applicant
RenovoRx, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2017
Days to Decision
419 days
Submission Type
Summary