CENTRIA T4 RIA TEST SET— 510(k) K790800

Name: FDA 510(k) clearance K790800
Creator: U.S. Food and Drug Administration
Published: 1979-06-15

Substantially Equivalent

Ventrex Laboratories, Inc.

FDA 510(k) clearance K790800 for CENTRIA T4 RIA TEST SET, Substantially Equivalent on 1979-06-15. Applicant: Ventrex Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Ventrex Laboratories, Inc.
Product code: Code CDX
Device class: Class 2
Regulation: 21 CFR 862.1700
Advisory panel: Clinical Chemistry
Date received: 1979-04-24
Decision date: 1979-06-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CDX

view all

K961490 — ELECSYS T4 ASSAY1996-06-13
K954312 — ACTIVE THYROXINE RIA1995-10-07
K943416 — DELFIA NEONATAL THYROXINE KIT1995-03-10
K934384 — AXSYM(TM) TOTAL T41994-06-21
K932980 — TOTAL T4 FPIA REAGENT SET/CALIBRATOR #T-1039,T-1161993-10-18

More clearances from Ventrex Laboratories, Inc.

view all

K914554 — SPECIFIC IGE EIA-TURBO ASSAY1992-03-13
K913833 — VENTREX ALLERGEN DISC1992-02-21
K913434 — VENTREX COATED TUBE INTACT PTH1991-10-25
K905612 — VENTREX COATED TUBE IGE RADIOIMMUNOASSAY1991-02-21
K905636 — VENTREX COATED TUBE IGE ENZYME IMMUNOASSAY1991-02-07

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