JBAIDS Q FEVER DETECTION KIT— 510(k) K103207

Name: FDA 510(k) clearance K103207
Creator: U.S. Food and Drug Administration
Published: 2011-05-20

Substantially Equivalent

Idaho Technology, Inc.

FDA 510(k) clearance K103207 for JBAIDS Q FEVER DETECTION KIT, Substantially Equivalent on 2011-05-20. Applicant: Idaho Technology, Inc.. Device class: 1.

Clearance details

Applicant: Idaho Technology, Inc.
Product code: Code OVF
Device class: Class 1
Regulation: 21 CFR 866.3500
Advisory panel: Microbiology
Date received: 2010-11-01
Decision date: 2011-05-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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