LITHIUM DILUENT (1500 MM/E)— 510(k) K800039

Name: FDA 510(k) clearance K800039
Creator: U.S. Food and Drug Administration
Published: 1980-01-21

Substantially Equivalent

Gilford Diagnostics

FDA 510(k) clearance K800039 for LITHIUM DILUENT (1500 MM/E), Substantially Equivalent on 1980-01-21. Applicant: Gilford Diagnostics. Device class: 2.

Clearance details

Applicant: Gilford Diagnostics
Product code: Code JIH
Device class: Class 2
Regulation: 21 CFR 862.3560
Advisory panel: Clinical Toxicology
Date received: 1980-01-07
Decision date: 1980-01-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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More clearances from Gilford Diagnostics

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K832094 — BILIRUBIN CALIBRATORS & CONTROL1983-08-11
K831843 — GILCHEM TOTAL BILIRUBIN REAGENT1983-07-18
K831844 — DIRECT BILIRUBIN REAGENT1983-07-18
K823709 — TRIGLYCERIDE REAGENT (UV)1983-01-07
K822739 — AHBD1982-10-18

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