Last synced on 25 April 2025 at 11:05 pm

800 SERIES SURGICAL LASER SYSTEM AND ACCCESSORIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970948
510(k) Type
Traditional
Applicant
LASERSCOPE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/1997
Days to Decision
68 days
Submission Type
Summary

800 SERIES SURGICAL LASER SYSTEM AND ACCCESSORIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970948
510(k) Type
Traditional
Applicant
LASERSCOPE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/1997
Days to Decision
68 days
Submission Type
Summary