LIGHT DIAGNOSTICS HUMAN METAPNEUMOVIRUS DFA KIT, MODEL CATALOG NUMBER 3124— 510(k) K093815

Name: FDA 510(k) clearance K093815
Creator: U.S. Food and Drug Administration
Published: 2010-03-12

Substantially Equivalent

Millipore Corporation

FDA 510(k) clearance K093815 for LIGHT DIAGNOSTICS HUMAN METAPNEUMOVIRUS DFA KIT, MODEL CATALOG NUMBER 3124, Substantially Equivalent on 2010-03-12. Applicant: Millipore Corporation. Device class: 2.

Clearance details

Applicant: Millipore Corporation
Product code: Code OMG
Device class: Class 2
Regulation: 21 CFR 866.3980
Advisory panel: Microbiology
Date received: 2009-12-14
Decision date: 2010-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Temecula, CA, US

Download summary PDF View on FDA.gov ↗

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