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MODIFICATION TO INTRALASE 600C LASER KERATOME

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001211
510(k) Type
Traditional
Applicant
Intra Lase Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/2000
Days to Decision
234 days
Submission Type
Summary

MODIFICATION TO INTRALASE 600C LASER KERATOME

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001211
510(k) Type
Traditional
Applicant
Intra Lase Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/2000
Days to Decision
234 days
Submission Type
Summary