IQ TUPTAKE ASSAY— 510(k) K931294

Name: FDA 510(k) clearance K931294
Creator: U.S. Food and Drug Administration
Published: 1993-07-22

Substantially Equivalent

Becton Dickinson Advanced Diagnostics

FDA 510(k) clearance K931294 for IQ TUPTAKE ASSAY, Substantially Equivalent on 1993-07-22. Applicant: Becton Dickinson Advanced Diagnostics. Device class: 2.

Clearance details

Applicant: Becton Dickinson Advanced Diagnostics
Product code: Code KHQ
Device class: Class 2
Regulation: 21 CFR 862.1715
Advisory panel: Clinical Chemistry
Date received: 1993-03-15
Decision date: 1993-07-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sparks, MD, US

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K961488 — ELECSYS T-UPTAKE ASSAY1996-06-12

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