510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K941642Substantially Equivalent

Ascenda

American Stair-Glide Corp., Grandview MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K941642 is the FDA 510(k) clearance record for ASCENDA, a class II device, cleared for American Stair-Glide Corp. 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 2 510(k) clearances for American Stair-Glide Corp., from to . As of , FDA records show no recalls naming K941642.

Clearance record

Decision date
Received
(70 days to decision)
Product code
ING Elevator, Wheelchair, Portable
Regulation
21 CFR 890.3930
Device class
Class II
Review panel
Physical Medicine
Applicant
American Stair-Glide Corp. 4001 E. 138th St., Grandview MO
510(k) summary
Statement
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