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MODIFIED COHERENT ULTRAPULSE CO2 SURGICAL LASERS

Page Type
Cleared 510(K)
510(k) Number
K951812
510(k) Type
Traditional
Applicant
LUMENIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/1995
Days to Decision
79 days
Submission Type
Summary

MODIFIED COHERENT ULTRAPULSE CO2 SURGICAL LASERS

Page Type
Cleared 510(K)
510(k) Number
K951812
510(k) Type
Traditional
Applicant
LUMENIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/1995
Days to Decision
79 days
Submission Type
Summary