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AURORA DS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041969
510(k) Type
Traditional
Applicant
SYNERON MEDICAL LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
10/19/2004
Days to Decision
89 days
Submission Type
Summary

AURORA DS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041969
510(k) Type
Traditional
Applicant
SYNERON MEDICAL LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
10/19/2004
Days to Decision
89 days
Submission Type
Summary