Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Power Mobility Scooter (MJMA01, MJMA02)

K-Number: K253936 · 2026-03-12

Decision Date2026-03-12
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Power Mobility Scooter (MJMA01, MJMA02) is a medical device manufactured by Nanjing Mijo Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-03-12 under approval number K253936. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Power Mobility Scooter (MJMA01, MJMA02)?

Power Mobility Scooter (MJMA01, MJMA02) is a medical device that received FDA 510(k) clearance on 2026-03-12. It is manufactured by Nanjing Mijo Technology Co., Ltd.. The 510(k) number is K253936.

When was Power Mobility Scooter (MJMA01, MJMA02) approved by the FDA?

Power Mobility Scooter (MJMA01, MJMA02) received FDA 510(k) clearance on 2026-03-12, under approval number K253936.

What company makes Power Mobility Scooter (MJMA01, MJMA02)?

Power Mobility Scooter (MJMA01, MJMA02) is manufactured by Nanjing Mijo Technology Co., Ltd..

What is the FDA product code for Power Mobility Scooter (MJMA01, MJMA02)?

The FDA product code for Power Mobility Scooter (MJMA01, MJMA02) is INI.

Related Clinical Trials

Related Devices (Code: INI)

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.