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ANGELITE FAMILY OF INTENSE PULSED LIGHT SYSTEMS, MODELS ANGELITE-DDC AND ANGELITE-SDC

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083915
510(k) Type
Traditional
Applicant
ADVANCED TECHNOLOGY LASER CO., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
1/29/2009
Days to Decision
30 days
Submission Type
Statement

ANGELITE FAMILY OF INTENSE PULSED LIGHT SYSTEMS, MODELS ANGELITE-DDC AND ANGELITE-SDC

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083915
510(k) Type
Traditional
Applicant
ADVANCED TECHNOLOGY LASER CO., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
1/29/2009
Days to Decision
30 days
Submission Type
Statement