ILUMIEN OPTIS— 510(k) K123369
Substantially EquivalentLightlab Imaging, Inc.
FDA 510(k) clearance K123369 for ILUMIEN OPTIS, Substantially Equivalent on 2013-01-30. Applicant: Lightlab Imaging, Inc.. Device class: 2.
Clearance details
- Applicant
- Lightlab Imaging, Inc.
- Product code
- Code NQQ
- Device class
- Class 2
- Regulation
- 21 CFR 892.1560
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Westford, MA, US
Recent devices under product code NQQ
view allMore clearances from Lightlab Imaging, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.