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FDA 510(k)

Electronic Pulse Stimulator

K-Number: K160508 · 2016-11-21

ApplicantBeijing Choice Electronic Technololgy Co., Ltd.
Decision Date2016-11-21
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Electronic Pulse Stimulator is a medical device manufactured by Beijing Choice Electronic Technololgy Co., Ltd.. It received FDA 510(k) clearance on 2016-11-21 under approval number K160508. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Electronic Pulse Stimulator?

Electronic Pulse Stimulator is a medical device that received FDA 510(k) clearance on 2016-11-21. It is manufactured by Beijing Choice Electronic Technololgy Co., Ltd.. The 510(k) number is K160508.

When was Electronic Pulse Stimulator approved by the FDA?

Electronic Pulse Stimulator received FDA 510(k) clearance on 2016-11-21, under approval number K160508.

What company makes Electronic Pulse Stimulator?

Electronic Pulse Stimulator is manufactured by Beijing Choice Electronic Technololgy Co., Ltd..

What is the FDA product code for Electronic Pulse Stimulator?

The FDA product code for Electronic Pulse Stimulator is NUH.

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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.

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