JBAIDS TULAREMIA DETECTION KIT, MODEL JRPD-ASY-0124— 510(k) K072547

Name: FDA 510(k) clearance K072547
Creator: U.S. Food and Drug Administration
Published: 2007-12-19

Substantially Equivalent

Idaho Technology, Inc.

FDA 510(k) clearance K072547 for JBAIDS TULAREMIA DETECTION KIT, MODEL JRPD-ASY-0124, Substantially Equivalent on 2007-12-19. Applicant: Idaho Technology, Inc.. Device class: 2.

Clearance details

Applicant: Idaho Technology, Inc.
Product code: Code OEH
Device class: Class 2
Regulation: 21 CFR 866.3280
Advisory panel: Microbiology
Date received: 2007-09-10
Decision date: 2007-12-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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