Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K921444Substantially Equivalent

Digi Sportlens System

Fitness Quest, Inc., Canton OH / Traditional, Substantially Equivalent

K921444 is the FDA 510(k) clearance record for DIGI SPORTLENS SYSTEM, a class I device, cleared for Fitness Quest, Inc. on under FDA product code HQY (Sunglasses (Non-Prescription Including Photosensitive)). FDA records list 2 510(k) clearances for Fitness Quest, Inc., from to . As of , FDA records show no recalls naming K921444.

Clearance record

Decision date
Received
(110 days to decision)
Product code
HQY Sunglasses (Non-Prescription Including Photosensitive)
Regulation
21 CFR 886.5850
Device class
Class I
Review panel
Ophthalmic
Applicant
Fitness Quest, Inc. 1375 Raff Rd. SW, Canton OH
510(k) summary
Statement
Third party review
No

Clearances, product code HQY

Trailing 12 months

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

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