510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K770611Substantially Equivalent

Parallel Bars

Will Ross Co., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K770611 is the FDA 510(k) clearance record for PARALLEL BARS, a class I device, cleared for Will Ross Co. on under FDA product code IOE (Bars, Parallel, Exercise). FDA records list 14 510(k) clearances for Will Ross Co., from to . As of , FDA records show no recalls naming K770611.

Clearance record

Decision date
Received
(8 days to decision)
Product code
IOE Bars, Parallel, Exercise
Regulation
21 CFR 890.5370
Device class
Class I
Review panel
Physical Medicine
Applicant
Will Ross Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code IOE

Trailing 12 months

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

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