Electronic stimulator
K-Number: K200354 · 2020-06-29
Decision Date2020-06-29
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Electronic stimulator is a medical device manufactured by Shenzhen Dongjilian Electronics Co., Ltd.. It received FDA 510(k) clearance on 2020-06-29 under approval number K200354. 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 stimulator?
Electronic stimulator is a medical device that received FDA 510(k) clearance on 2020-06-29. It is manufactured by Shenzhen Dongjilian Electronics Co., Ltd.. The 510(k) number is K200354.
When was Electronic stimulator approved by the FDA?
Electronic stimulator received FDA 510(k) clearance on 2020-06-29, under approval number K200354.
What company makes Electronic stimulator?
Electronic stimulator is manufactured by Shenzhen Dongjilian Electronics Co., Ltd..
What is the FDA product code for Electronic stimulator?
The FDA product code for Electronic stimulator is NUH.
Other Devices by Shenzhen Dongjilian Electronics Co., Ltd.
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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.