510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K926054Substantially Equivalent

Eld-Arondak Chair

Al'S Woodcraft, Inc., Borden IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K926054 is the FDA 510(k) clearance record for ELD-ARONDAK CHAIR, a class I device, cleared for Al'S Woodcraft, Inc. on under FDA product code INM (Chair, With Casters). FDA records list one 510(k) clearance for Al'S Woodcraft, Inc. As of , FDA records show no recalls naming K926054.

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
Al'S Woodcraft, Inc. P.O. Box 117, 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