Last synced on 25 January 2026 at 3:41 am

FIDELIS PLUS III D, AT FIDELIS D, POWERLASE AT D / FIDELIS PLUS III, AT FIDELIS, POWERLASE AT / FIDELIS ER III D, HT FID

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093162
510(k) Type
Traditional
Applicant
Fotona D.D.
Country
Slovenia
FDA Decision
Substantially Equivalent
Decision Date
1/22/2010
Days to Decision
108 days
Submission Type
Summary

FIDELIS PLUS III D, AT FIDELIS D, POWERLASE AT D / FIDELIS PLUS III, AT FIDELIS, POWERLASE AT / FIDELIS ER III D, HT FID

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093162
510(k) Type
Traditional
Applicant
Fotona D.D.
Country
Slovenia
FDA Decision
Substantially Equivalent
Decision Date
1/22/2010
Days to Decision
108 days
Submission Type
Summary