510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K901381Substantially Equivalent

Superarm 2000 Lift

Handicaps, Inc., Englewood CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K901381 is the FDA 510(k) clearance record for SUPERARM 2000 LIFT, a class II device, cleared for Handicaps, Inc. on under FDA product code ING (Elevator, Wheelchair, Portable). FDA's definition for product code ING reads: "A motorized lift device that is not permanently mounted in one location and that is intended for medical purposes to provide a means to move a person with impaired mobility, with or without a wheelchair, from one level to another (e.g...". FDA records list one 510(k) clearance for Handicaps, Inc. As of , FDA records show no recalls naming K901381.

Clearance record

Decision date
Received
(25 days to decision)
Product code
ING Elevator, Wheelchair, Portable
Regulation
21 CFR 890.3930
Device class
Class II
Review panel
Physical Medicine
Applicant
Handicaps, Inc. 4335 S. Santa Fe Dr., Englewood CO
Third party review
No

Clearances, product code ING

Trailing 12 months

FDA records hold no clearances under product code ING in the trailing twelve months.

FDA records show no clearances under product code ING in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code ING, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260