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. The listed applicant is Innovasis, Inc.. The 510(k) number is K200874.
When did TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal End receive FDA 510(k) clearance?
TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal End received FDA 510(k) clearance on 2020-06-30, under 510(k) number K200874.
Who is the listed applicant for TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal End?
The FDA 510(k) record lists Innovasis, Inc. as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Innovasis, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.