CYCLIC AMP RADIOIMMUNOASSAY KIT [125I]— 510(k) K811273

Name: FDA 510(k) clearance K811273
Creator: U.S. Food and Drug Administration
Published: 1981-05-27

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K811273 for CYCLIC AMP RADIOIMMUNOASSAY KIT [125I], Substantially Equivalent on 1981-05-27. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 2.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code CHO
Device class: Class 2
Regulation: 21 CFR 862.1230
Advisory panel: Clinical Chemistry
Date received: 1981-05-07
Decision date: 1981-05-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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K823504 — CYCLIC ADENOSINE MONOPHOSHATE BY RADIO1983-01-28
K811746 — KING DIAGNOSTICS CHOLESTEROL-FE TEST1981-07-10

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