510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K933311Substantially Equivalent

Motorized Electric Parallel Bars

Midland Mfg. Co., Great Neck NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K933311 is the FDA 510(k) clearance record for MOTORIZED ELECTRIC PARALLEL BARS, a class I device, cleared for Midland Mfg. Co. on under FDA product code BXB (Exerciser, Powered). FDA records list 7 510(k) clearances for Midland Mfg. Co., from to . As of , FDA records show no recalls naming K933311.

Clearance record

Decision date
Received
(203 days to decision)
Product code
BXB Exerciser, Powered
Regulation
21 CFR 890.5380
Device class
Class I
Review panel
Physical Medicine
Applicant
Midland Mfg. Co. 55 Northern Blvd., Suite 301, Great Neck NY
510(k) summary
Statement
Third party review
No

Clearances, product code BXB

Trailing 12 months

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

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