Wireless Pain Relieve Device Model: LT5018C
K-Number: K173462 · 2017-12-08
Device Summary
Frequently Asked Questions
What is the Wireless Pain Relieve Device Model: LT5018C?
Wireless Pain Relieve Device Model: LT5018C is a medical device that received FDA 510(k) clearance on 2017-12-08. The listed applicant is Shenzhen Dongdixin Technology Co., Ltd.. The 510(k) number is K173462.
When did Wireless Pain Relieve Device Model: LT5018C receive FDA 510(k) clearance?
Wireless Pain Relieve Device Model: LT5018C received FDA 510(k) clearance on 2017-12-08, under 510(k) number K173462.
Who is the listed applicant for Wireless Pain Relieve Device Model: LT5018C?
The FDA 510(k) record lists Shenzhen Dongdixin Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Wireless Pain Relieve Device Model: LT5018C?
The FDA product code for Wireless Pain Relieve Device Model: LT5018C is NUH.
Other records listing Shenzhen Dongdixin Technology 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.