Last synced on 25 January 2026 at 3:41 am

cmAngio® (V1.6)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250754
510(k) Type
Special
Applicant
Curemetrix, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/2025
Days to Decision
29 days
Submission Type
Statement

cmAngio® (V1.6)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250754
510(k) Type
Special
Applicant
Curemetrix, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/2025
Days to Decision
29 days
Submission Type
Statement