FDA 510(k)

Soniquence Reusable Neutral Plate

K-Number: K220071 · 2022-02-03

Decision Date2022-02-03

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

Soniquence Reusable Neutral Plate is a medical device manufactured by Soniquence, LLC. It received FDA 510(k) clearance on 2022-02-03 under approval number K220071. 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 Soniquence Reusable Neutral Plate?

Soniquence Reusable Neutral Plate is a medical device that received FDA 510(k) clearance on 2022-02-03. It is manufactured by Soniquence, LLC. The 510(k) number is K220071.

When was Soniquence Reusable Neutral Plate approved by the FDA?

Soniquence Reusable Neutral Plate received FDA 510(k) clearance on 2022-02-03, under approval number K220071.

What company makes Soniquence Reusable Neutral Plate?

Soniquence Reusable Neutral Plate is manufactured by Soniquence, LLC.

What is the FDA product code for Soniquence Reusable Neutral Plate?

The FDA product code for Soniquence Reusable Neutral Plate is GEI.

Other Devices by Soniquence, LLC

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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.