AUTODELFIA NEONATAL IRT L KIT, MODEL B022-112— 510(k) K070889

Name: FDA 510(k) clearance K070889
Creator: U.S. Food and Drug Administration
Published: 2008-04-14

Substantially Equivalent

Wallac OY

FDA 510(k) clearance K070889 for AUTODELFIA NEONATAL IRT L KIT, MODEL B022-112, Substantially Equivalent on 2008-04-14. Applicant: Wallac OY. Device class: 2.

Clearance details

Applicant: Wallac OY
Product code: Code CGZ
Device class: Class 2
Regulation: 21 CFR 862.1170
Advisory panel: Clinical Chemistry
Date received: 2007-03-30
Decision date: 2008-04-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Turku, FI

Download summary PDF View on FDA.gov ↗

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