ASSAY SYSTEM, FERRITIN I KIT— 510(k) K781888

Name: FDA 510(k) clearance K781888
Creator: U.S. Food and Drug Administration
Published: 1979-01-10

Substantially Equivalent

New England Nuclear

FDA 510(k) clearance K781888 for ASSAY SYSTEM, FERRITIN I KIT, Substantially Equivalent on 1979-01-10. Applicant: New England Nuclear. Device class: 2.

Clearance details

Applicant: New England Nuclear
Product code: Code JMG
Device class: Class 2
Regulation: 21 CFR 866.5340
Advisory panel: Immunology
Date received: 1978-11-07
Decision date: 1979-01-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JMG

view all

K234052 — Access Ferritin2024-03-20
K052082 — FERRITIN ON THE ACCESS IMMUNOASSAY SYSTEMS, MODEL 330202005-08-19
K964282 — TINA-QUANT FERRITIN ASSAY1997-07-30
K971833 — ELECSYS FERRITIN1997-06-02
K963498 — FERR FLEX REAGENT CARTRIDGE1997-01-24

More clearances from New England Nuclear

view all

K841478 — RIANEN CYCLIC-AMP RADIOIMMUNOASSAY1984-06-14
K840301 — RIANEN ESTRIOL RADIOIMMUNOASSAY KIT1984-03-30
K834038 — RIANEN FOLLICLE STIMULATING HORMONE1984-01-30
K833376 — RIANEN LUTEINIZING HORMONE RIA KIT1983-12-20
K831345 — RIANEN PROLACTIN 125I KIT1983-06-08

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