TOXOPLASMA GONDII ANTIBODY IGG— 510(k) K822605

Substantially Equivalent

Immulok, Inc.

FDA 510(k) clearance K822605 for TOXOPLASMA GONDII ANTIBODY IGG, Substantially Equivalent on 1982-10-27. Applicant: Immulok, Inc.. Device class: 2.

Clearance details

Applicant: Immulok, Inc.
Product code: Code LJK
Device class: Class 2
Regulation: 21 CFR 866.3780
Advisory panel: Microbiology
Date received: 1982-08-27
Decision date: 1982-10-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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