510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K932240Substantially Equivalent

Model 5200-10,5200-12 Hi-Low Elec. Parrallel Bars

Bailey Mfg. Co., Lodi OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K932240 is the FDA 510(k) clearance record for MODEL 5200-10,5200-12 HI-LOW ELEC. PARRALLEL BARS, a class I device, cleared for Bailey Mfg. Co. on under FDA product code IRR (Bars, Parallel, Powered). FDA records list 11 510(k) clearances for Bailey Mfg. Co., from to . As of , FDA records show no recalls naming K932240.

Clearance record

Decision date
Received
(329 days to decision)
Product code
IRR Bars, Parallel, Powered
Regulation
21 CFR 890.5380
Device class
Class I
Review panel
Physical Medicine
Applicant
Bailey Mfg. Co. P.O. Box 130, Lodi OH
510(k) summary
Statement
Third party review
No

Clearances, product code IRR

Trailing 12 months

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

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