Ellusa Reusable Bipolar Cable
K-Number: K222429 · 2022-09-09
ApplicantEllusa, LLC
Decision Date2022-09-09
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Ellusa Reusable Bipolar Cable is a medical device manufactured by Ellusa, LLC. It received FDA 510(k) clearance on 2022-09-09 under approval number K222429. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Ellusa Reusable Bipolar Cable?
Ellusa Reusable Bipolar Cable is a medical device that received FDA 510(k) clearance on 2022-09-09. It is manufactured by Ellusa, LLC. The 510(k) number is K222429.
When was Ellusa Reusable Bipolar Cable approved by the FDA?
Ellusa Reusable Bipolar Cable received FDA 510(k) clearance on 2022-09-09, under approval number K222429.
What company makes Ellusa Reusable Bipolar Cable?
Ellusa Reusable Bipolar Cable is manufactured by Ellusa, LLC.
What is the FDA product code for Ellusa Reusable Bipolar Cable?
The FDA product code for Ellusa Reusable Bipolar Cable is GEI.
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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.