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SURGILASE FIBERLASE CO2 LASER WAVEGUIDE

Page Type
Cleared 510(K)
510(k) Number
K924664
510(k) Type
Traditional
Applicant
SURGILASE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/1993
Days to Decision
226 days
Submission Type
Statement

SURGILASE FIBERLASE CO2 LASER WAVEGUIDE

Page Type
Cleared 510(K)
510(k) Number
K924664
510(k) Type
Traditional
Applicant
SURGILASE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/1993
Days to Decision
226 days
Submission Type
Statement