LDH REAGENT SET— 510(k) K812836

Unknown

Anco Medical Reagents & Assoc.

FDA 510(k) clearance K812836 for LDH REAGENT SET, Unknown on 1981-10-09. Applicant: Anco Medical Reagents & Assoc.. Device class: 2.

Clearance details

Applicant: Anco Medical Reagents & Assoc.
Product code: Code CFH
Device class: Class 2
Regulation: 21 CFR 862.1440
Advisory panel: Clinical Chemistry
Date received: 1981-10-09
Decision date: 1981-10-09
Decision: Unknown
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Anco Medical Reagents & Assoc.

K842440 — SICKLE CELL STAT A/S HETEROZYGOUS-ERYTH1984-07-27
K831871 — SICKLE-HEME A/S CONTROLS & A/A CONTROL1983-07-28
K821658 — HEMOGLOBIN REAGENT1982-06-25
K821526 — ACID PHOSPHATASE REAGENT SET1982-06-10
K821102 — MEGNESIUM REAGENT KIT1982-05-05

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