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SurBlate Ablation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223272
510(k) Type
Traditional
Applicant
Mima-Pro Scientific Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
2/28/2023
Days to Decision
127 days
Submission Type
Summary

SurBlate Ablation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223272
510(k) Type
Traditional
Applicant
Mima-Pro Scientific Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
2/28/2023
Days to Decision
127 days
Submission Type
Summary