Electronic Pulse Stimulator
K-Number: K221992 · 2022-10-21
Decision Date2022-10-21
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Electronic Pulse Stimulator is a medical device manufactured by Beijing Choice Electronic Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-10-21 under approval number K221992. 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 2022-10-21. It is manufactured by Beijing Choice Electronic Technology Co., Ltd.. The 510(k) number is K221992.
When was Electronic Pulse Stimulator approved by the FDA?
Electronic Pulse Stimulator received FDA 510(k) clearance on 2022-10-21, under approval number K221992.
What company makes Electronic Pulse Stimulator?
Electronic Pulse Stimulator is manufactured by Beijing Choice Electronic Technology 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.