Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K930624Substantially Equivalent

Sanitas Whirpool Bathing System

Dutton-Lainson Co., Hastings NE / Traditional, Substantially Equivalent

K930624 is the FDA 510(k) clearance record for SANITAS WHIRPOOL BATHING SYSTEM, a class II device, cleared for Dutton-Lainson Co. on under FDA product code ILJ (Bath, Hydro-Massage). FDA records list 3 510(k) clearances for Dutton-Lainson Co., from to . As of , FDA records show no recalls naming K930624.

Clearance record

Decision date
Received
(508 days to decision)
Product code
ILJ Bath, Hydro-Massage
Regulation
21 CFR 890.5100
Device class
Class II
Review panel
Physical Medicine
Applicant
Dutton-Lainson Co. 451 W. Second St., Hastings NE
510(k) summary
Statement
Third party review
No

Clearances, product code ILJ

Trailing 12 months

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

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