Manual Wheelchair
K-Number: K220671 · 2022-07-21
Device Summary
Frequently Asked Questions
What is the Manual Wheelchair?
Manual Wheelchair is a medical device that received FDA 510(k) clearance on 2022-07-21. The listed applicant is Hebei Ruilangde Medical Equipment Technology Group Co., Ltd.. The 510(k) number is K220671.
When did Manual Wheelchair receive FDA 510(k) clearance?
Manual Wheelchair received FDA 510(k) clearance on 2022-07-21, under 510(k) number K220671.
Who is the listed applicant for Manual Wheelchair?
The FDA 510(k) record lists Hebei Ruilangde Medical Equipment Technology Group Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Manual Wheelchair?
The FDA product code for Manual Wheelchair is IOR.
Related Clinical Trials
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: IOR)
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.