Last synced on 25 April 2025 at 11:05 pm

MODIFICATION TO AURORA DS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033586
510(k) Type
Special
Applicant
SYNERON MEDICAL LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
12/10/2003
Days to Decision
27 days
Submission Type
Summary

MODIFICATION TO AURORA DS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033586
510(k) Type
Special
Applicant
SYNERON MEDICAL LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
12/10/2003
Days to Decision
27 days
Submission Type
Summary