Needle Stimulator
K-Number: K202861 · 2021-08-27
Device Summary
Frequently Asked Questions
What is the Needle Stimulator?
Needle Stimulator is a medical device that received FDA 510(k) clearance on 2021-08-27. The listed applicant is Wuxi Jiajian Medical Instrument Co., Ltd.. The 510(k) number is K202861.
When did Needle Stimulator receive FDA 510(k) clearance?
Needle Stimulator received FDA 510(k) clearance on 2021-08-27, under 510(k) number K202861.
Who is the listed applicant for Needle Stimulator?
The FDA 510(k) record lists Wuxi Jiajian Medical Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Needle Stimulator?
The FDA product code for Needle Stimulator is BWK.
Other records listing Wuxi Jiajian Medical Instrument 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.