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MODIFICATION TO: LASERPRO 810, 940, AND 980 DIODE DIODE LASER SYSTEMS

Page Type
Cleared 510(K)
510(k) Number
K042211
510(k) Type
Traditional
Applicant
SURGICAL LASER TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2004
Days to Decision
84 days
Submission Type
Summary

MODIFICATION TO: LASERPRO 810, 940, AND 980 DIODE DIODE LASER SYSTEMS

Page Type
Cleared 510(K)
510(k) Number
K042211
510(k) Type
Traditional
Applicant
SURGICAL LASER TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2004
Days to Decision
84 days
Submission Type
Summary