Needle Stimulator
K-Number: K202861 · 2021-08-27
Decision Date2021-08-27
Product CodeBWK
DecisionSubstantially Equivalent
Device Summary
Needle Stimulator is a medical device manufactured by Wuxi Jiajian Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2021-08-27 under approval number K202861. The device is classified under product code BWK. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Needle Stimulator?
Needle Stimulator is a medical device that received FDA 510(k) clearance on 2021-08-27. It is manufactured by Wuxi Jiajian Medical Instrument Co., Ltd.. The 510(k) number is K202861.
When was Needle Stimulator approved by the FDA?
Needle Stimulator received FDA 510(k) clearance on 2021-08-27, under approval number K202861.
What company makes Needle Stimulator?
Needle Stimulator is manufactured by Wuxi Jiajian Medical Instrument Co., Ltd..
What is the FDA product code for Needle Stimulator?
The FDA product code for Needle Stimulator is BWK.
Other Devices by Wuxi Jiajian Medical Instrument Co., Ltd.
Related Devices (Code: BWK)
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.