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
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K926053Substantially Equivalent

Eld-Arondak Chair

Alert Care, Inc., Borden IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K926053 is the FDA 510(k) clearance record for ELD-ARONDAK CHAIR, a class I device, cleared for Alert Care, Inc. on under FDA product code INM (Chair, With Casters). FDA records list one 510(k) clearance for Alert Care, Inc. As of , FDA records show no recalls naming K926053.

Clearance record

Decision date
Received
(111 days to decision)
Product code
INM Chair, With Casters
Regulation
21 CFR 890.3100
Device class
Class I
Review panel
Physical Medicine
Applicant
Alert Care, Inc. C/O Al'S Woodcraft, Borden IN
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