Last synced on 23 May 2025 at 11:06 pm

MySegmenter (v2.0.0)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242647
510(k) Type
Traditional
Applicant
MySegmenter Technologies Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/2025
Days to Decision
225 days
Submission Type
Summary

MySegmenter (v2.0.0)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242647
510(k) Type
Traditional
Applicant
MySegmenter Technologies Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/2025
Days to Decision
225 days
Submission Type
Summary