Muscle Stimulator
K-Number: K231648 · 2024-03-01
Device Summary
Frequently Asked Questions
What is the Muscle Stimulator?
Muscle Stimulator is a medical device that received FDA 510(k) clearance on 2024-03-01. The listed applicant is Shenzhen Yiran Intelligent Co., Ltd.. The 510(k) number is K231648.
When did Muscle Stimulator receive FDA 510(k) clearance?
Muscle Stimulator received FDA 510(k) clearance on 2024-03-01, under 510(k) number K231648.
Who is the listed applicant for Muscle Stimulator?
The FDA 510(k) record lists Shenzhen Yiran Intelligent Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Muscle Stimulator?
The FDA product code for Muscle Stimulator is NUH.
Related Clinical Trials
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.