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SURGILASE FIBERLASE VCO2 LASER WAVEGUIDE

Page Type
Cleared 510(K)
510(k) Number
K921671
510(k) Type
Traditional
Applicant
SURGICAL PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/1992
Days to Decision
71 days
Submission Type
Statement

SURGILASE FIBERLASE VCO2 LASER WAVEGUIDE

Page Type
Cleared 510(K)
510(k) Number
K921671
510(k) Type
Traditional
Applicant
SURGICAL PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/1992
Days to Decision
71 days
Submission Type
Statement