FDA 510(k)

Trigger Switch and Cord

K-Number: K200455 · 2020-03-31

Decision Date2020-03-31

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

Trigger Switch and Cord is a medical device manufactured by New Deantronics Taiwan , Ltd.. It received FDA 510(k) clearance on 2020-03-31 under approval number K200455. 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 Trigger Switch and Cord?

Trigger Switch and Cord is a medical device that received FDA 510(k) clearance on 2020-03-31. It is manufactured by New Deantronics Taiwan , Ltd.. The 510(k) number is K200455.

When was Trigger Switch and Cord approved by the FDA?

Trigger Switch and Cord received FDA 510(k) clearance on 2020-03-31, under approval number K200455.

What company makes Trigger Switch and Cord?

Trigger Switch and Cord is manufactured by New Deantronics Taiwan , Ltd..

What is the FDA product code for Trigger Switch and Cord?

The FDA product code for Trigger Switch and Cord 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.