Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K925839Substantially Equivalent

Trackmaster

Jas Manufacturing Co., Inc., Carrollton TX / Traditional, Substantially Equivalent

K925839 is the FDA 510(k) clearance record for TRACKMASTER, a class I device, cleared for Jas Manufacturing Co., Inc. on under FDA product code IOL (Treadmill, Powered). FDA records list one 510(k) clearance for Jas Manufacturing Co., Inc. As of , FDA records show no recalls naming K925839.

Clearance record

Decision date
Received
(218 days to decision)
Product code
IOL Treadmill, Powered
Regulation
21 CFR 890.5380
Device class
Class I
Review panel
Physical Medicine
Applicant
Jas Manufacturing Co., Inc. 3228 Skylane Dr., Carrollton TX
510(k) summary
Statement
Third party review
No

Clearances, product code IOL

Trailing 12 months

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

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