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ORION SERIES SURGICAL LASER SYSTEM (Q-SWITCHED ND:YAG CONFIGURATION)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964818
510(k) Type
Traditional
Applicant
LASERSCOPE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/1997
Days to Decision
200 days
Submission Type
Summary

ORION SERIES SURGICAL LASER SYSTEM (Q-SWITCHED ND:YAG CONFIGURATION)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964818
510(k) Type
Traditional
Applicant
LASERSCOPE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/1997
Days to Decision
200 days
Submission Type
Summary