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ACUPULSE 30/40 ST CO2 LASER SYSTEM AND ACUPULSE 40WG CO2 LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100415
510(k) Type
Traditional
Applicant
LUMENIS
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
4/21/2010
Days to Decision
64 days
Submission Type
Summary

ACUPULSE 30/40 ST CO2 LASER SYSTEM AND ACUPULSE 40WG CO2 LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100415
510(k) Type
Traditional
Applicant
LUMENIS
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
4/21/2010
Days to Decision
64 days
Submission Type
Summary