Electric Scooter (M2085, S2091)
K-Number: K240272 · 2024-07-16
Device Summary
Frequently Asked Questions
What is the Electric Scooter (M2085, S2091)?
Electric Scooter (M2085, S2091) is a medical device that received FDA 510(k) clearance on 2024-07-16. The listed applicant is Guangdong Prestige Technology Co., Ltd.. The 510(k) number is K240272.
When did Electric Scooter (M2085, S2091) receive FDA 510(k) clearance?
Electric Scooter (M2085, S2091) received FDA 510(k) clearance on 2024-07-16, under 510(k) number K240272.
Who is the listed applicant for Electric Scooter (M2085, S2091)?
The FDA 510(k) record lists Guangdong Prestige Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Electric Scooter (M2085, S2091)?
The FDA product code for Electric Scooter (M2085, S2091) is INI.
Other records listing Guangdong Prestige 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: 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.