Last synced on 23 May 2025 at 11:06 pm

In Reach

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170789
510(k) Type
Traditional
Applicant
CurveBeam, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/2017
Days to Decision
50 days
Submission Type
Summary

In Reach

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170789
510(k) Type
Traditional
Applicant
CurveBeam, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/2017
Days to Decision
50 days
Submission Type
Summary