HEMOGLOBIN CONTROLS— 510(k) K790310

Substantially Equivalent

Electrophoresis Corp.

FDA 510(k) clearance K790310 for HEMOGLOBIN CONTROLS, Substantially Equivalent on 1979-03-21. Applicant: Electrophoresis Corp.. Device class: 2.

Clearance details

Applicant: Electrophoresis Corp.
Product code: Code GGM
Device class: Class 2
Regulation: 21 CFR 864.8625
Advisory panel: Hematology
Date received: 1979-02-13
Decision date: 1979-03-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GGM

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K070546 — LYPHOCHEK DIABETES CONTROL2007-04-02
K070334 — R&D SICKLE QC CONTROL2007-03-29
K052838 — LIQUICHEK DIABETES CONTROL, LEVEL 1,2,3,42005-11-09

More clearances from Electrophoresis Corp.

K802395 — SPECIAL PROCEDURE AQAROSE FILM1980-11-26
K790309 — CPK ISOENZYME SUBSTRATE1979-04-04
K790311 — LDH ISOENZYME REAGENT1979-03-21

Data sourced from openFDA. This site is unofficial and independent of the FDA.