510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K821198Substantially Equivalent

Direct Glucose Reagent Set

Omega Medical Electronics, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K821198 is the FDA 510(k) clearance record for DIRECT GLUCOSE REAGENT SET, a class II device, cleared for Omega Medical Electronics on under FDA product code CGE (Orthotoluidine, Glucose). FDA records list 21 510(k) clearances for Omega Medical Electronics, from to . As of , FDA records show no recalls naming K821198.

Clearance record

Decision date
Received
(77 days to decision)
Product code
CGE Orthotoluidine, Glucose
Regulation
21 CFR 862.1345
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Omega Medical Electronics 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code CGE

Trailing 12 months

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

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