BUN REAGENT— 510(k) K800341

Substantially Equivalent

Gilford Diagnostics

FDA 510(k) clearance K800341 for BUN REAGENT, Substantially Equivalent on 1980-03-12. Applicant: Gilford Diagnostics. Device class: 2.

Clearance details

Applicant: Gilford Diagnostics
Product code: Code CDQ
Device class: Class 2
Regulation: 21 CFR 862.1770
Advisory panel: Clinical Chemistry
Date received: 1980-02-15
Decision date: 1980-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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More clearances from Gilford Diagnostics

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

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