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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
K031988
510(k) Type
Special
Applicant
SYNERON MEDICAL LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
8/1/2003
Days to Decision
35 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
K031988
510(k) Type
Special
Applicant
SYNERON MEDICAL LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
8/1/2003
Days to Decision
35 days
Submission Type
Summary