510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K841302Substantially Equivalent

Diagnon Folate 125I Ria Kit

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

K841302 is the FDA 510(k) clearance record for DIAGNON FOLATE 125I RIA KIT, a class II device, cleared for Diagnon Corp. on under FDA product code CGN (Acid, Folic, Radioimmunoassay). FDA records list 6 510(k) clearances for Diagnon Corp., from to . As of , FDA records show no recalls naming K841302.

Clearance record

Decision date
Received
(84 days to decision)
Product code
CGN Acid, Folic, Radioimmunoassay
Regulation
21 CFR 862.1295
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Diagnon Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code CGN

Trailing 12 months

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

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