510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K061116Substantially Equivalent

Mobillife - Model (Mobil Raizer 22) - Power Wheelchair

Mobilife, LLC, Delafield WI / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)

K061116 is the FDA 510(k) clearance record for MOBILLIFE - MODEL (MOBIL RAIZER 22) - POWER WHEELCHAIR, a class II device, cleared for Mobilife, LLC 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 one 510(k) clearance for Mobilife, LLC. As of , FDA records show no recalls naming K061116.

Clearance record

Decision date
Received
(73 days to decision)
Product code
ITI Wheelchair, Powered
Regulation
21 CFR 890.3860
Device class
Class II
Review panel
Physical Medicine
Applicant
Mobilife, LLC 78 Enterprise Rd., Delafield WI
510(k) summary
Statement
Third party review
No

Clearances, product code ITI

Trailing 12 months
39 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 20265
October 20262