510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K890039Substantially Equivalent

Kleen Test Basin Set

Kleen Test Products Corporation, Elkhorn WI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K890039 is the FDA 510(k) clearance record for KLEEN TEST BASIN SET, a class II device, cleared for Kleen Test Products on under FDA product code JOL (Catheter And Tip, Suction). FDA records list 17 510(k) clearances for Kleen Test Products, from to . As of , FDA records show no recalls naming K890039.

Clearance record

Decision date
Received
(287 days to decision)
Product code
JOL Catheter And Tip, Suction
Regulation
21 CFR 880.6740
Device class
Class II
Review panel
General Hospital
Applicant
Kleen Test Products P.O. Box 140, Elkhorn WI
Third party review
No

Clearances, product code JOL

Trailing 12 months

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

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