ZEUS SCIENTIFIC, INC VZV IGM ELISA TEST SYSTEM— 510(k) K070317

Name: FDA 510(k) clearance K070317
Creator: U.S. Food and Drug Administration
Published: 2007-07-05

Substantially Equivalent

Zeus Scientific, Inc.

FDA 510(k) clearance K070317 for ZEUS SCIENTIFIC, INC VZV IGM ELISA TEST SYSTEM, Substantially Equivalent on 2007-07-05. Applicant: Zeus Scientific, Inc.. Device class: 2.

Clearance details

Applicant: Zeus Scientific, Inc.
Product code: Code LFY
Device class: Class 2
Regulation: 21 CFR 866.3900
Advisory panel: Microbiology
Date received: 2007-02-02
Decision date: 2007-07-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Branchburg, NJ, US

Download summary PDF View on FDA.gov ↗

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