Needle Stimulator (Model: RJNS6-1)
K-Number: K220153 · 2022-03-18
Device Summary
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. The listed applicant is Bozhou Rongjian Medical Appliance Co., Ltd.. The 510(k) number is K220153.
When did Needle Stimulator (Model: RJNS6-1) receive FDA 510(k) clearance?
Needle Stimulator (Model: RJNS6-1) received FDA 510(k) clearance on 2022-03-18, under 510(k) number K220153.
Who is the listed applicant for Needle Stimulator (Model: RJNS6-1)?
The FDA 510(k) record lists Bozhou Rongjian Medical Appliance Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Needle Stimulator (Model: RJNS6-1)?
The FDA product code for Needle Stimulator (Model: RJNS6-1) is BWK.
Other records listing Bozhou Rongjian Medical Appliance Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: BWK)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.