AGGLUTINOTEST-TOXOPLASMOSIS— 510(k) K791456

Name: FDA 510(k) clearance K791456
Creator: U.S. Food and Drug Administration
Published: 1979-09-24

Substantially Equivalent

Volu Sol Medical Industries

FDA 510(k) clearance K791456 for AGGLUTINOTEST-TOXOPLASMOSIS, Substantially Equivalent on 1979-09-24. Applicant: Volu Sol Medical Industries. Device class: 2.

Clearance details

Applicant: Volu Sol Medical Industries
Product code: Code GMN
Device class: Class 2
Regulation: 21 CFR 866.3780
Advisory panel: Microbiology
Date received: 1979-08-06
Decision date: 1979-09-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GMN

view all

K894261 — TOXOPLASMA GONDII-CF ANTIGEN AND CONTROL ANTIGEN1989-10-16
K864981 — TOXOPLASMA GONDII1987-10-30

More clearances from Volu Sol Medical Industries

view all

K822126 — VOLU-SOL CARNOY FLUID1982-08-05
K822127 — VOLU-SOL ZENKERS FIXATIVE1982-08-05
K822128 — VOLU-SOL SINGLE DIFFERENTIAL STAIN1982-08-05
K822129 — VOLU-SOL BOVINS FIXATIVE1982-08-05
K822035 — VOLU-SOL GILLS EA1982-08-03

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