ELECTRIC WHEELCHAIR (QDWP-A01,QDWP-B02)
K-Number: K251248 · 2025-06-20
ApplicantJinhua Qidian Vehicle Co., Ltd.
Decision Date2025-06-20
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
ELECTRIC WHEELCHAIR (QDWP-A01,QDWP-B02) is a medical device manufactured by Jinhua Qidian Vehicle Co., Ltd.. It received FDA 510(k) clearance on 2025-06-20 under approval number K251248. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ELECTRIC WHEELCHAIR (QDWP-A01,QDWP-B02)?
ELECTRIC WHEELCHAIR (QDWP-A01,QDWP-B02) is a medical device that received FDA 510(k) clearance on 2025-06-20. It is manufactured by Jinhua Qidian Vehicle Co., Ltd.. The 510(k) number is K251248.
When was ELECTRIC WHEELCHAIR (QDWP-A01,QDWP-B02) approved by the FDA?
ELECTRIC WHEELCHAIR (QDWP-A01,QDWP-B02) received FDA 510(k) clearance on 2025-06-20, under approval number K251248.
What company makes ELECTRIC WHEELCHAIR (QDWP-A01,QDWP-B02)?
ELECTRIC WHEELCHAIR (QDWP-A01,QDWP-B02) is manufactured by Jinhua Qidian Vehicle Co., Ltd..
What is the FDA product code for ELECTRIC WHEELCHAIR (QDWP-A01,QDWP-B02)?
The FDA product code for ELECTRIC WHEELCHAIR (QDWP-A01,QDWP-B02) is ITI.
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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.