OPTILUX 501— 510(k) K020091
Substantially EquivalentKerr Corporation (Danbury)
FDA 510(k) clearance K020091 for OPTILUX 501, Substantially Equivalent on 2002-03-21. Applicant: Kerr Corporation (Danbury). Device class: 2.
Clearance details
- Applicant
- Kerr Corporation (Danbury)
- Product code
- Code EBZ
- Device class
- Class 2
- Regulation
- 21 CFR 872.6070
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Orange, CA, US
Recent devices under product code EBZ
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