MODIFICATION TO JBAIDS ANTHRAX DETECTION SYSTEM— 510(k) K071188

Name: FDA 510(k) clearance K071188
Creator: U.S. Food and Drug Administration
Published: 2007-05-21

Substantially Equivalent

Idaho Technology, Inc.

FDA 510(k) clearance K071188 for MODIFICATION TO JBAIDS ANTHRAX DETECTION SYSTEM, Substantially Equivalent on 2007-05-21. Applicant: Idaho Technology, Inc.. Device class: 2.

Clearance details

Applicant: Idaho Technology, Inc.
Product code: Code NHT
Device class: Class 2
Regulation: 21 CFR 866.3045
Advisory panel: Microbiology
Date received: 2007-04-30
Decision date: 2007-05-21
Decision: Substantially Equivalent
Clearance type: Special
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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