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MYDON C

Page Type
Cleared 510(K)
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)
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