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FOTONA FIDELIS III ER:YAG/ND:YAG LASER SYSTEM FAMILY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070355
510(k) Type
Traditional
Applicant
FOTONA D.D.
Country
Slovenia
FDA Decision
Substantially Equivalent
Decision Date
3/4/2008
Days to Decision
392 days
Submission Type
Summary

FOTONA FIDELIS III ER:YAG/ND:YAG LASER SYSTEM FAMILY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070355
510(k) Type
Traditional
Applicant
FOTONA D.D.
Country
Slovenia
FDA Decision
Substantially Equivalent
Decision Date
3/4/2008
Days to Decision
392 days
Submission Type
Summary