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ALLEGRO OCULYZER

Page Type
Cleared 510(K)
510(k) Number
K071183
510(k) Type
Traditional
Applicant
Wavelight AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
7/20/2007
Days to Decision
81 days
Submission Type
Summary

ALLEGRO OCULYZER

Page Type
Cleared 510(K)
510(k) Number
K071183
510(k) Type
Traditional
Applicant
Wavelight AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
7/20/2007
Days to Decision
81 days
Submission Type
Summary