ALLEGRO OCULYZER— 510(k) K071183
Substantially EquivalentWavelight AG
FDA 510(k) clearance K071183 for ALLEGRO OCULYZER, Substantially Equivalent on 2007-07-20. Applicant: Wavelight AG. Device class: 2.
Clearance details
- Applicant
- Wavelight AG
- Product code
- Code MXK
- Device class
- Class 2
- Regulation
- 21 CFR 886.1850
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Erlangen, DE
Recent devices under product code MXK
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