510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K840787Substantially Equivalent

Craftmatic Electric Adjustable Bed

Contour, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K840787 is the FDA 510(k) clearance record for CRAFTMATIC ELECTRIC ADJUSTABLE BED, a class II device, cleared for Contour, Inc. on under FDA product code LLI (Bed, Therapeutic, Ac-Powered, Adjustable Home-Use). FDA records list one 510(k) clearance for Contour, Inc. As of , FDA records show no recalls naming K840787.

Clearance record

Decision date
Received
(145 days to decision)
Product code
LLI Bed, Therapeutic, Ac-Powered, Adjustable Home-Use
Regulation
21 CFR 880.5100
Device class
Class II
Review panel
General Hospital
Applicant
Contour, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code LLI

Trailing 12 months

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

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