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MODIFICATION TO EPI-STAR SURGICAL LASER SYSTEM, M0DEL DS-60

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013864
510(k) Type
Traditional
Applicant
Nidek, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/2002
Days to Decision
79 days
Submission Type
Summary

MODIFICATION TO EPI-STAR SURGICAL LASER SYSTEM, M0DEL DS-60

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013864
510(k) Type
Traditional
Applicant
Nidek, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/2002
Days to Decision
79 days
Submission Type
Summary