VibrantVue Scleral Saline
K-Number: K201069 · 2020-07-31
ApplicantDry Eye Innovations, LLC
Decision Date2020-07-31
Product CodeMRC
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
VibrantVue Scleral Saline is a medical device manufactured by Dry Eye Innovations, LLC. It received FDA 510(k) clearance on 2020-07-31 under approval number K201069. The device is classified under product code MRC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the VibrantVue Scleral Saline?
VibrantVue Scleral Saline is a medical device that received FDA 510(k) clearance on 2020-07-31. It is manufactured by Dry Eye Innovations, LLC. The 510(k) number is K201069.
When was VibrantVue Scleral Saline approved by the FDA?
VibrantVue Scleral Saline received FDA 510(k) clearance on 2020-07-31, under approval number K201069.
What company makes VibrantVue Scleral Saline?
VibrantVue Scleral Saline is manufactured by Dry Eye Innovations, LLC.
What is the FDA product code for VibrantVue Scleral Saline?
The FDA product code for VibrantVue Scleral Saline is MRC.
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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.