510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K860543Substantially Equivalent

Blood Urea Nitrogen (Bun) Testcard

Ilex Corp., Attleboro MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K860543 is the FDA 510(k) clearance record for BLOOD UREA NITROGEN (BUN) TESTCARD, a class II device, cleared for Ilex Corp. on under FDA product code CDS (Electrode, Ion Specific, Urea Nitrogen). FDA records list 3 510(k) clearances for Ilex Corp., from to . As of , FDA records show no recalls naming K860543.

Clearance record

Decision date
Received
(67 days to decision)
Product code
CDS Electrode, Ion Specific, Urea Nitrogen
Regulation
21 CFR 862.1770
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Ilex Corp. C/O Medical Device Consultants, Attleboro MA
Third party review
No

Clearances, product code CDS

Trailing 12 months

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

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