Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K905227Substantially Equivalent

Glucose (Hk) Reagent, Universal

Enzyme Technology, Inc., Shelton CT / Traditional, Substantially Equivalent

K905227 is the FDA 510(k) clearance record for GLUCOSE (HK) REAGENT, UNIVERSAL, a class II device, cleared for Enzyme Technology, Inc. on under FDA product code CFR (Hexokinase, Glucose). FDA records list 5 510(k) clearances for Enzyme Technology, Inc., from to . As of , FDA records show no recalls naming K905227.

Clearance record

Decision date
Received
(111 days to decision)
Product code
CFR Hexokinase, Glucose
Regulation
21 CFR 862.1345
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Enzyme Technology, Inc. 415 Howe Ave., Shelton CT
Third party review
No

Clearances, product code CFR

Trailing 12 months
1 clearance under product code CFR in the twelve months to October 2026, February 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CFR, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260