510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K031898Substantially Equivalent

Ekf Diagnostic Hemo Control Hemoglobin Measurement System

Ekf Diagnostic GmbH, Egale WI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K031898 is the FDA 510(k) clearance record for EKF DIAGNOSTIC HEMO CONTROL HEMOGLOBIN MEASUREMENT SYSTEM, a class II device, cleared for Ekf Diagnostic GmbH on under FDA product code GKR (System, Hemoglobin, Automated). FDA records list 5 510(k) clearances for Ekf Diagnostic GmbH, from to . As of , FDA records show no recalls naming K031898.

Clearance record

Decision date
Received
(97 days to decision)
Product code
GKR System, Hemoglobin, Automated
Regulation
21 CFR 864.5620
Device class
Class II
Review panel
Hematology
Applicant
Ekf Diagnostic GmbH S65w35739 Piper Rd., Egale WI
510(k) summary
Statement
Third party review
No

Clearances, product code GKR

Trailing 12 months

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

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