Lightlab Imaging, Inc.
Lightlab Imaging, Inc. holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2016.
Top product codes for Lightlab Imaging, Inc.
Recent clearances by Lightlab Imaging, Inc.
- K160878 — OPTIS Metallic Stent Optimization E.4 SW
- K152120 — OPTIS Mobile System
- K151286 — OPTIS Integrated System Mobile Workstation
- K150878 — ILUMIEN OPTIS
- K150237 — ILUMIEN, Drageonfly OPTIS Imaging Catheter
- K141453 — ILUMIEN OPTIS, DRAGONFLY OPTIS IMAGING CATHETER
- K141769 — OPTIS INTEGRATED SYSTEM, DRAGONFLY OPTIS IMAGING CATHETER
- K123369 — ILUMIEN OPTIS
- K111201 — C7 XR IMAGING SYSTEM
- K093857 — C7 XR IMAGING SYSTEM WITH C7 DRAGONFLY IMAGING CATHETER AND DISPOSABLE ACCESSORIES
Data sourced from openFDA. This site is unofficial and independent of the FDA.