510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K893032Substantially Equivalent

Pacer R 9 Treadmill

Pacer Industries, Inc., Carrollton TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K893032 is the FDA 510(k) clearance record for PACER R 9 TREADMILL, a class I device, cleared for Pacer Industries, Inc. on under FDA product code IOL (Treadmill, Powered). FDA records list one 510(k) clearance for Pacer Industries, Inc. As of , FDA records show no recalls naming K893032.

Clearance record

Decision date
Received
(94 days to decision)
Product code
IOL Treadmill, Powered
Regulation
21 CFR 890.5380
Device class
Class I
Review panel
Physical Medicine
Applicant
Pacer Industries, Inc. 1121 Crowley Rd., Carrollton TX
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