Electronic stimulator
K-Number: K200354 · 2020-06-29
Device Summary
Frequently Asked Questions
What is the Electronic stimulator?
Electronic stimulator is a medical device that received FDA 510(k) clearance on 2020-06-29. The listed applicant is Shenzhen Dongjilian Electronics Co., Ltd.. The 510(k) number is K200354.
When did Electronic stimulator receive FDA 510(k) clearance?
Electronic stimulator received FDA 510(k) clearance on 2020-06-29, under 510(k) number K200354.
Who is the listed applicant for Electronic stimulator?
The FDA 510(k) record lists Shenzhen Dongjilian Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Electronic stimulator?
The FDA product code for Electronic stimulator is NUH.
Other records listing Shenzhen Dongjilian Electronics 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.