Electrical Stimulator System
K-Number: K232439 · 2024-03-21
Device Summary
Frequently Asked Questions
What is the Electrical Stimulator System?
Electrical Stimulator System is a medical device that received FDA 510(k) clearance on 2024-03-21. The listed applicant is Gymmax Technology Shenzen Co., Ltd.. The 510(k) number is K232439.
When did Electrical Stimulator System receive FDA 510(k) clearance?
Electrical Stimulator System received FDA 510(k) clearance on 2024-03-21, under 510(k) number K232439.
Who is the listed applicant for Electrical Stimulator System?
The FDA 510(k) record lists Gymmax Technology Shenzen Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Electrical Stimulator System?
The FDA product code for Electrical Stimulator System is NUH.
Other records listing Gymmax Technology Shenzen 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: 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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.