TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal End
K-Number: K200874 · 2020-06-30
Device Summary
Frequently Asked Questions
What is the TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal End?
TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal End is a medical device that received FDA 510(k) clearance on 2020-06-30. It is manufactured by Innovasis, Inc.. The 510(k) number is K200874.
When was TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal End approved by the FDA?
TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal End received FDA 510(k) clearance on 2020-06-30, under approval number K200874.
What company makes TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal End?
TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal End is manufactured by Innovasis, Inc..
What is the FDA product code for TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal End?
The FDA product code for TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal End is FST.
Related Clinical Trials
Other Devices by Innovasis, Inc.
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.