510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K926361Substantially Equivalent

Glucometer Encore Qa Blood Glucose Meter

Kulzer GmbH, Mishawaka IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K926361 is the FDA 510(k) clearance record for GLUCOMETER ENCORE QA BLOOD GLUCOSE METER, a class II device, cleared for Heraeus Kulzer, Inc. on under FDA product code CFR (Hexokinase, Glucose). FDA records list 205 510(k) clearances for KULZER GMBH, from to . As of , FDA records show no recalls naming K926361.

Clearance record

Decision date
Received
(185 days to decision)
Product code
CFR Hexokinase, Glucose
Regulation
21 CFR 862.1345
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Heraeus Kulzer, Inc. P.O. Box 2004, Mishawaka IN
510(k) summary
Summary
Third party review
No

Clearances, product code CFR

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