Electronic Pulse Stimulator
K-Number: K183674 · 2019-10-11
Device Summary
Frequently Asked Questions
What is the Electronic Pulse Stimulator?
Electronic Pulse Stimulator is a medical device that received FDA 510(k) clearance on 2019-10-11. The listed applicant is Shenzhen Leading Perfection Technology Co., Ltd.. The 510(k) number is K183674.
When did Electronic Pulse Stimulator receive FDA 510(k) clearance?
Electronic Pulse Stimulator received FDA 510(k) clearance on 2019-10-11, under 510(k) number K183674.
Who is the listed applicant for Electronic Pulse Stimulator?
The FDA 510(k) record lists Shenzhen Leading Perfection Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Electronic Pulse Stimulator?
The FDA product code for Electronic Pulse Stimulator is NUH.
Related Devices (Code: NUH)
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
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