510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K840284Substantially Equivalent

Multiple Sys-Urine Drainage-Closed

Luth Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K840284 is the FDA 510(k) clearance record for MULTIPLE SYS-URINE DRAINAGE-CLOSED, a class II device, cleared for Luth Corp. on under FDA product code KNX (Collector, Urine, (And Accessories) For Indwelling Catheter). FDA records list 2 510(k) clearances for Luth Corp. As of , FDA records show no recalls naming K840284.

Clearance record

Decision date
Received
(86 days to decision)
Product code
KNX Collector, Urine, (And Accessories) For Indwelling Catheter
Regulation
21 CFR 876.5250
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Luth Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KNX

Trailing 12 months

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

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