Manual Wheelchair
K-Number: K220671 · 2022-07-21
Decision Date2022-07-21
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Manual Wheelchair is a medical device manufactured by Hebei Ruilangde Medical Equipment Technology Group Co., Ltd.. It received FDA 510(k) clearance on 2022-07-21 under approval number K220671. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Manual Wheelchair?
Manual Wheelchair is a medical device that received FDA 510(k) clearance on 2022-07-21. It is manufactured by Hebei Ruilangde Medical Equipment Technology Group Co., Ltd.. The 510(k) number is K220671.
When was Manual Wheelchair approved by the FDA?
Manual Wheelchair received FDA 510(k) clearance on 2022-07-21, under approval number K220671.
What company makes Manual Wheelchair?
Manual Wheelchair is manufactured by Hebei Ruilangde Medical Equipment Technology Group Co., Ltd..
What is the FDA product code for Manual Wheelchair?
The FDA product code for Manual Wheelchair is IOR.
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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.