510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K792362Substantially Equivalent

Blood Urea Nitrogen Reagent

Connecticut Diagnostics, Ltd., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K792362 is the FDA 510(k) clearance record for BLOOD UREA NITROGEN REAGENT, a class II device, cleared for Connecticut Diagnostics, Ltd. on under FDA product code JGZ (O-Phthalaldehyde, Urea Nitrogen). FDA records list 14 510(k) clearances for Connecticut Diagnostics, Ltd., from to . As of , FDA records show no recalls naming K792362.

Clearance record

Decision date
Received
(15 days to decision)
Product code
JGZ O-Phthalaldehyde, Urea Nitrogen
Regulation
21 CFR 862.1770
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Connecticut Diagnostics, Ltd. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JGZ

Trailing 12 months

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

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