Needle Stimulator (Model: RJNS6-1)
K-Number: K220153 · 2022-03-18
Decision Date2022-03-18
Product CodeBWK
DecisionSubstantially Equivalent
Device Summary
Needle Stimulator (Model: RJNS6-1) is a medical device manufactured by Bozhou Rongjian Medical Appliance Co., Ltd.. It received FDA 510(k) clearance on 2022-03-18 under approval number K220153. The device is classified under product code BWK. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Needle Stimulator (Model: RJNS6-1)?
Needle Stimulator (Model: RJNS6-1) is a medical device that received FDA 510(k) clearance on 2022-03-18. It is manufactured by Bozhou Rongjian Medical Appliance Co., Ltd.. The 510(k) number is K220153.
When was Needle Stimulator (Model: RJNS6-1) approved by the FDA?
Needle Stimulator (Model: RJNS6-1) received FDA 510(k) clearance on 2022-03-18, under approval number K220153.
What company makes Needle Stimulator (Model: RJNS6-1)?
Needle Stimulator (Model: RJNS6-1) is manufactured by Bozhou Rongjian Medical Appliance Co., Ltd..
What is the FDA product code for Needle Stimulator (Model: RJNS6-1)?
The FDA product code for Needle Stimulator (Model: RJNS6-1) is BWK.
Related Clinical Trials
Other Devices by Bozhou Rongjian Medical Appliance 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.