K100327 is an FDA 510(k) clearance for the HEARTWAY POWER CHAIR, P23. This device is classified as a Wheelchair, Powered (Class II - Special Controls, product code ITI).
Submitted by Heartway Medical Products Co., Ltd. (Hsin Chu City,,, Tw Hsq, TW). The FDA issued a Cleared decision on March 22, 2010, 46 days after receiving the submission on February 4, 2010.
This device falls under the Physical Medicine FDA review panel. Regulated under 21 CFR 890.3860. A Powered Wheelchair Is A Battery-operated Device With Wheels That Is Intended For Medical Purposes To Provide Mobility To Persons Restricted To A Sitting Position. Fda Interprets mobility To Persons Restricted To A Sitting Position To Mean The Device Type Is Intended To Provide Mobility To Individuals Who Have Mobility Impairments And Require An Assistive Device For Mobility. Note: This Type Of Device Is Not Intended To Climb Stairs (see Product Code: Imk)..