510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K933000Substantially Equivalent

Reclining Geri Chairs W/casters & Lap Tray

Winco, Inc., Ocala FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K933000 is the FDA 510(k) clearance record for RECLINING GERI CHAIRS W/CASTERS & LAP TRAY, a class I device, cleared for Winco, Inc. on under FDA product code INM (Chair, With Casters). FDA records list 3 510(k) clearances for Winco, Inc., from to . As of , FDA records show no recalls naming K933000.

Clearance record

Decision date
Received
(104 days to decision)
Product code
INM Chair, With Casters
Regulation
21 CFR 890.3100
Device class
Class I
Review panel
Physical Medicine
Applicant
Winco, Inc. 5516 SW First Ln., Ocala FL
510(k) summary
Statement
Third party review
No

Clearances, product code INM

Trailing 12 months

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

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