510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K950324Substantially Equivalent

Multi-Wash

Multi-Wash Medical, Ltd., Marysville MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K950324 is the FDA 510(k) clearance record for MULTI-WASH, a class I device, cleared for Multi-Wash Medical, Ltd. on under FDA product code LRJ (Disinfectant, Medical Devices). FDA records list one 510(k) clearance for Multi-Wash Medical, Ltd. As of , FDA records show no recalls naming K950324.

Clearance record

Decision date
Received
(72 days to decision)
Product code
LRJ Disinfectant, Medical Devices
Regulation
21 CFR 880.6890
Device class
Class I
Review panel
General Hospital
Applicant
Multi-Wash Medical, Ltd. 2829 Gratiot Blvd., Suite A, Marysville MI
510(k) summary
Statement
Third party review
No

Clearances, product code LRJ

Trailing 12 months

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

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