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cmAngio® V1.0

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232367
510(k) Type
Traditional
Applicant
CureMetrix, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2023
Days to Decision
58 days
Submission Type
Statement

cmAngio® V1.0

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232367
510(k) Type
Traditional
Applicant
CureMetrix, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2023
Days to Decision
58 days
Submission Type
Statement