FIAX IGG TEST— 510(k) K832821

Substantially Equivalent

Intl. Diagnostic Technology

FDA 510(k) clearance K832821 for FIAX IGG TEST, Substantially Equivalent on 1983-10-14. Applicant: Intl. Diagnostic Technology. Device class: 1.

Clearance details

Applicant: Intl. Diagnostic Technology
Product code: Code DFI
Device class: Class 1
Regulation: 21 CFR 866.5860
Advisory panel: Immunology
Date received: 1983-08-19
Decision date: 1983-10-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Recent devices under product code DFI

K854190 — CANTROL SPINAL FLUID CONTROL1985-11-25
K843122 — RESOLVE-CSF1984-11-30
K840974 — SOMAS HUMAN SPINAL FLUID CONTROL1984-04-05

More clearances from Intl. Diagnostic Technology

K850591 — FIAX TOXO-M ANTIBODIES TEST KIT1985-04-30
K843570 — FIAX HAPTOGLOBIN TEST KIT1984-10-05
K843621 — FIAX 420 DILUTOR1984-09-28
K843356 — FIAX 100 FLUOROMETER1984-09-17
K842749 — FIAX TOTAL IGE TEST KIT1984-08-28

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