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800 SERIES SURGICAL LASER SYSTEM ORION SERIES SURGICAL LASER SYSTEM ANGLED DELIVERY DEVICES

Page Type
Cleared 510(K)
510(k) Number
K972575
510(k) Type
Traditional
Applicant
LASERSCOPE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/1998
Days to Decision
372 days
Submission Type
Summary

800 SERIES SURGICAL LASER SYSTEM ORION SERIES SURGICAL LASER SYSTEM ANGLED DELIVERY DEVICES

Page Type
Cleared 510(K)
510(k) Number
K972575
510(k) Type
Traditional
Applicant
LASERSCOPE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/1998
Days to Decision
372 days
Submission Type
Summary