510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K253806Substantially Equivalent

Power Wheelchair (N5919 series)

Zhejiang Innuovo Rehabilitation Devices Co., Ltd., Dongyang, CN / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K253806 is the FDA 510(k) clearance record for Power Wheelchair (N5919 series), a class II device, cleared for Zhejiang Innuovo Rehabilitation Devices Co.,Ltd on under FDA product code ITI (Wheelchair, Powered). FDA's definition for product code ITI reads: "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...". FDA records list 20 510(k) clearances for Zhejiang Innuovo Rehabilitation Devices Co.,Ltd, from to . As of , FDA records show no recalls naming K253806.

Clearance record

Decision date
Received
(143 days to decision)
Product code
ITI Wheelchair, Powered
Regulation
21 CFR 890.3860
Device class
Class II
Review panel
Physical Medicine
Applicant
Zhejiang Innuovo Rehabilitation Devices Co.,Ltd #196 Industry Rd., Hengdian Movie Zone, Dongyang, CN
510(k) summary
Statement
Third party review
No

Clearances, product code ITI

Trailing 12 months
36 clearances under product code ITI in the twelve months to October 2026, March 2026 the highest month at 7.
Show the numbers
Monthly 510(k) clearances under FDA product code ITI, trailing twelve months
MonthClearances
November 20253
December 20253
January 20262
February 20263
March 20267
April 20263
May 20261
June 20266
July 20263
August 20261
September 20264
October 20260