510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K990866Substantially Equivalent

Quinton Medtrack Cr Plus Treadmill

Quinton, Inc., Bothell WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K990866 is the FDA 510(k) clearance record for QUINTON MEDTRACK CR PLUS TREADMILL, a class II device, cleared for Quinton, Inc. on under FDA product code ISD (Exerciser, Measuring). FDA records list 164 510(k) clearances for Quinton, Inc., from to . As of , FDA records show one recall naming K990866.

Clearance record

Decision date
Received
(44 days to decision)
Product code
ISD Exerciser, Measuring
Regulation
21 CFR 890.5360
Device class
Class II
Review panel
Physical Medicine
Applicant
Quinton, Inc. 3303 Monte Villa Pkwy., Bothell WA
510(k) summary
Statement
Third party review
No

Clearances, product code ISD

Trailing 12 months

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

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