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Rulo Radiofrequency Lesion Probe

Page Type
Cleared 510(K)
510(k) Number
K190256
510(k) Type
Traditional
Applicant
Epimed International, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2019
Days to Decision
29 days
Submission Type
Summary

Rulo Radiofrequency Lesion Probe

Page Type
Cleared 510(K)
510(k) Number
K190256
510(k) Type
Traditional
Applicant
Epimed International, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2019
Days to Decision
29 days
Submission Type
Summary