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FDA 510(k)

TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal End

K-Number: K200874 · 2020-06-30

Decision Date2020-06-30
Product CodeFST
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal End is a medical device manufactured by Innovasis, Inc.. It received FDA 510(k) clearance on 2020-06-30 under approval number K200874. The device is classified under product code FST. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.