VOLU-SOL DECALCIFER— 510(k) K822036

Name: FDA 510(k) clearance K822036
Creator: U.S. Food and Drug Administration
Published: 1982-08-03

Substantially Equivalent

Volu Sol Medical Industries

FDA 510(k) clearance K822036 for VOLU-SOL DECALCIFER, Substantially Equivalent on 1982-08-03. Applicant: Volu Sol Medical Industries. Device class: 1.

Clearance details

Applicant: Volu Sol Medical Industries
Product code: Code KDX
Device class: Class 1
Regulation: 21 CFR 864.4010
Advisory panel: Pathology
Date received: 1982-07-12
Decision date: 1982-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KDX

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K872625 — DECALCIFYING SOLUTION1987-08-06
K850636 — SIMUTANEOUS FIXATION & DECALCIFYING SOLUTION CAL-E1985-03-20
K842726 — DECALCIFIER SOLUTION1984-08-03
K841488 — DECALCIFIER I1984-05-02
K821443 — FORMICAL1982-06-02

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.