Last synced on 23 May 2025 at 11:06 pm

LineUp

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180727
510(k) Type
Traditional
Applicant
CurveBeam, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/2018
Days to Decision
52 days
Submission Type
Summary

LineUp

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180727
510(k) Type
Traditional
Applicant
CurveBeam, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/2018
Days to Decision
52 days
Submission Type
Summary