Scooter (YD-03)
K-Number: K253600 · 2026-06-03
Device Summary
Frequently Asked Questions
What is the Scooter (YD-03)?
Scooter (YD-03) is a medical device that received FDA 510(k) clearance on 2026-06-03. The listed applicant is Yurob Rehabilitation Medical Co., Ltd.. The 510(k) number is K253600.
When did Scooter (YD-03) receive FDA 510(k) clearance?
Scooter (YD-03) received FDA 510(k) clearance on 2026-06-03, under 510(k) number K253600.
Who is the listed applicant for Scooter (YD-03)?
The FDA 510(k) record lists Yurob Rehabilitation Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Scooter (YD-03)?
The FDA product code for Scooter (YD-03) is INI.
Other records listing Yurob Rehabilitation Medical 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: INI)
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.