ILUMIEN OPTIS— 510(k) K123369

Substantially Equivalent

Lightlab Imaging, Inc.

FDA 510(k) clearance K123369 for ILUMIEN OPTIS, Substantially Equivalent on 2013-01-30. Applicant: Lightlab Imaging, Inc..

Clearance details

Applicant: Lightlab Imaging, Inc.
Product code: Code NQQ
Advisory panel: Radiology
Date received: 2012-11-01
Decision date: 2013-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Westford, MA, US

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