Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K890577Substantially Equivalent

Kenlor Liquid Urine Control

Kenlor Industries, Inc., Westminster CA / Traditional, Substantially Equivalent

K890577 is the FDA 510(k) clearance record for KENLOR LIQUID URINE CONTROL, a class I device, cleared for Kenlor Industries, Inc. on under FDA product code JJW (Urinalysis Controls (Assayed And Unassayed)). FDA records list 9 510(k) clearances for Kenlor Industries, Inc., from to . As of , FDA records show no recalls naming K890577.

Clearance record

Decision date
Received
(31 days to decision)
Product code
JJW Urinalysis Controls (Assayed And Unassayed)
Regulation
21 CFR 862.1660
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Kenlor Industries, Inc. 8130 Mcfadden Ave., Suite 105, Westminster CA
Third party review
No

Clearances, product code JJW

Trailing 12 months

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

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