510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K823247Substantially Equivalent

U-Way Quickollar

Ems Industries, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K823247 is the FDA 510(k) clearance record for U-WAY QUICKOLLAR, a class I device, cleared for Ems Industries, Inc. on under FDA product code IQK (Orthosis, Cervical). FDA records list 2 510(k) clearances for Ems Industries, Inc., from to . As of , FDA records show no recalls naming K823247.

Clearance record

Decision date
Received
(15 days to decision)
Product code
IQK Orthosis, Cervical
Regulation
21 CFR 890.3490
Device class
Class I
Review panel
Physical Medicine
Applicant
Ems Industries, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code IQK

Trailing 12 months

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

FDA records show no clearances under product code IQK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code IQK, 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