Last synced on 10 January 2025 at 11:05 pm

Voyant Fine Fusion Device (EB230)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202818
510(k) Type
Traditional
Applicant
Applied Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2021
Days to Decision
448 days
Submission Type
Summary

Voyant Fine Fusion Device (EB230)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202818
510(k) Type
Traditional
Applicant
Applied Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2021
Days to Decision
448 days
Submission Type
Summary