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ACUPULSE 30 AND 40 CARBON DIOXIDE LASER SYSTEM

Page Type
Cleared 510(K)
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)
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