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ACUPULSE 30 AND 40 CARBON DIOXIDE LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082809
510(k) Type
Traditional
Applicant
LUMENIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2008
Days to Decision
85 days
Submission Type
Summary

ACUPULSE 30 AND 40 CARBON DIOXIDE LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082809
510(k) Type
Traditional
Applicant
LUMENIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2008
Days to Decision
85 days
Submission Type
Summary