Last synced on 25 April 2025 at 11:05 pm

MYDON C

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040384
510(k) Type
Traditional
Applicant
WAVELIGHT LASER TECHNOLOGIE AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2004
Days to Decision
87 days
Submission Type
Summary

MYDON C

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040384
510(k) Type
Traditional
Applicant
WAVELIGHT LASER TECHNOLOGIE AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2004
Days to Decision
87 days
Submission Type
Summary