Electronic Pulse Stimulator
K-Number: K160508 · 2016-11-21
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 2016-11-21. The listed applicant is Beijing Choice Electronic Technololgy Co., Ltd.. The 510(k) number is K160508.
When did Electronic Pulse Stimulator receive FDA 510(k) clearance?
Electronic Pulse Stimulator received FDA 510(k) clearance on 2016-11-21, under 510(k) number K160508.
Who is the listed applicant for Electronic Pulse Stimulator?
The FDA 510(k) record lists Beijing Choice Electronic Technololgy 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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