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VIVO

Page Type
Cleared 510(K)
510(k) Number
K183195
510(k) Type
Traditional
Applicant
Catheter Precision, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/2019
Days to Decision
207 days
Submission Type
Summary

VIVO

Page Type
Cleared 510(K)
510(k) Number
K183195
510(k) Type
Traditional
Applicant
Catheter Precision, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/2019
Days to Decision
207 days
Submission Type
Summary