AGGLUTINOTEST-RHEUMATOID ARTHRITIS— 510(k) K791507

Name: FDA 510(k) clearance K791507
Creator: U.S. Food and Drug Administration
Published: 1979-12-31

Substantially Equivalent

Volu Sol Medical Industries

FDA 510(k) clearance K791507 for AGGLUTINOTEST-RHEUMATOID ARTHRITIS, Substantially Equivalent on 1979-12-31. Applicant: Volu Sol Medical Industries. Device class: 2.

Clearance details

Applicant: Volu Sol Medical Industries
Product code: Code DHR
Device class: Class 2
Regulation: 21 CFR 866.5775
Advisory panel: Immunology
Date received: 1979-08-01
Decision date: 1979-12-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DHR

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K162263 — Optilite Rheumatoid Factor Kit2017-05-03
K160070 — Rheumatoid Factor (RF) Kit for use on SPAPLUS2016-12-07

More clearances from Volu Sol Medical Industries

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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.