Pantheris Catheter (8F), Pantheris Catheter (7F), Lightbox HS Imaging Console, Lightbox Sled
K-Number: K172236 · 2017-10-30
Device Summary
Frequently Asked Questions
What is the Pantheris Catheter (8F), Pantheris Catheter (7F), Lightbox HS Imaging Console, Lightbox Sled?
Pantheris Catheter (8F), Pantheris Catheter (7F), Lightbox HS Imaging Console, Lightbox Sled is a medical device that received FDA 510(k) clearance on 2017-10-30. It is manufactured by Avinger, Inc.. The 510(k) number is K172236.
When was Pantheris Catheter (8F), Pantheris Catheter (7F), Lightbox HS Imaging Console, Lightbox Sled approved by the FDA?
Pantheris Catheter (8F), Pantheris Catheter (7F), Lightbox HS Imaging Console, Lightbox Sled received FDA 510(k) clearance on 2017-10-30, under approval number K172236.
What company makes Pantheris Catheter (8F), Pantheris Catheter (7F), Lightbox HS Imaging Console, Lightbox Sled?
Pantheris Catheter (8F), Pantheris Catheter (7F), Lightbox HS Imaging Console, Lightbox Sled is manufactured by Avinger, Inc..
What is the FDA product code for Pantheris Catheter (8F), Pantheris Catheter (7F), Lightbox HS Imaging Console, Lightbox Sled?
The FDA product code for Pantheris Catheter (8F), Pantheris Catheter (7F), Lightbox HS Imaging Console, Lightbox Sled is MCW.
Related Clinical Trials
Other Devices by Avinger, Inc.
Related Devices (Code: MCW)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.