Electric Wheelchair (W-A807, W-A807L)
K-Number: K253599 · 2026-02-17
Device Summary
Frequently Asked Questions
What is the Electric Wheelchair (W-A807, W-A807L)?
Electric Wheelchair (W-A807, W-A807L) is a medical device that received FDA 510(k) clearance on 2026-02-17. The listed applicant is Ningbo Shenyu Medical Equipment Co.,Ltd. The 510(k) number is K253599.
When did Electric Wheelchair (W-A807, W-A807L) receive FDA 510(k) clearance?
Electric Wheelchair (W-A807, W-A807L) received FDA 510(k) clearance on 2026-02-17, under 510(k) number K253599.
Who is the listed applicant for Electric Wheelchair (W-A807, W-A807L)?
The FDA 510(k) record lists Ningbo Shenyu Medical Equipment Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Electric Wheelchair (W-A807, W-A807L)?
The FDA product code for Electric Wheelchair (W-A807, W-A807L) is ITI.
Other records listing Ningbo Shenyu Medical Equipment 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: ITI)
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.