510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K000102Substantially Equivalent

Glucose (Hexokinase) Liquid Reagent, Model G518-150

Teco Diagnostics, Anaheim CA / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K000102 is the FDA 510(k) clearance record for GLUCOSE (HEXOKINASE) LIQUID REAGENT, MODEL G518-150, a class II device, cleared for Teco Diagnostics on under FDA product code CFR (Hexokinase, Glucose). FDA records list 55 510(k) clearances for Teco Diagnostics, from to . As of , FDA records show no recalls naming K000102.

Clearance record

Decision date
Received
(26 days to decision)
Product code
CFR Hexokinase, Glucose
Regulation
21 CFR 862.1345
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Teco Diagnostics 4925 E. Hunter Ave., Anaheim CA
510(k) summary
Statement
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